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These entities are distinct from the amputations associated with constriction band syndrome weight loss 15 pounds order alli cheap online. Symbrachydactyly should be viewed as a clinical entity distinct from cleft hand weight loss pills qnexa uk purchase 60 mg alli visa, with a very different treatment plan. As Flatt (1) poignantly stated, "The cleft hand is a functional triumph and a social disaster. However, surgical closure of the cleft must be accompanied by appropriate treatment of the first web space and thumb to avoid functional compromise. The skin flaps designed for cleft closure, however, must take into account the status of the first web space. The adduction contracture of the thumb is released, and the index ray is transposed ulnarly at the same time. The SnowLittler, Ueba, and Miura flaps (320ͳ22) all involve transposition of the cleft skin to the first web space, with simultaneous transposition of the index ray ulnarly. If there is a transverse bone across the cleft, this must be removed in order to prevent progressive deformity. Often there is a conjoined flexor and extensor across the base of the cleft that has to be released. Associated fourth web space syndactylies are separated with Z-plasties and skin grafts. There may be associated camptodactyly or clinodactyly of the adjacent digits requiring corrective splinting or surgery. The treatment of symbrachydactyly in the United States is probably the most individualized of that of any of the congenital malformations. The range of options include (a) leaving the child alone, (b) nonvascularized transfers to the soft-tissue nubbins of the phalanges (323, 324), (c) microvascular toe transfer(s) (268, 325ͳ28), (d) web-space deepening, (e) digital distraction lengthening or bone grafting (329), and (f) use of a prosthesis. In addition, families and patients are very interested in the possibilities of transplantation and laboratory cellular growth of digits. There are few peer-reviewed published studies regarding functional and cosmetic outcomes that would guide the decision more objectively. However, there are clear principles to help guide all parties as to the best choice for them. In the presence of a normal thumb and web space, all of the choices for treatment will work. In this situation, treatment options focus on the quality of the other digital rays. If the soft-tissue pockets of the digits are adequate, nonvascularized transfer of the proximal phalanx of the toes is a very good choice. Although it will not provide normal digital length, it will provide stability for lateral pinch. This must be performed before 18 months of age and include the periosteum and collateral ligaments (323, 330). The proximal phalanx is harvested through an extensortendon-splitting dorsal approach. The proximal phalanx is harvested extraperiosteally, while protecting the neighboring tendons and neurovascular structures. At the metatarsophalangeal joint, the collateral ligaments, dorsal capsule, and volar plate are detached proximally from the metatarsal, while leaving intact their distal attachments to the phalanx. With transfer to the hand, the proximal soft tissues of the toe phalanx are sutured to the corresponding soft tissues of the recipient site. The best results for phalangeal survival and growth are realized when this procedure is performed before 1 year of age. In the presence of a normal thumb and first web, digital lengthening is another option. In addition, digital lengthening has been performed successfully after nonvascularized toe phalangeal transfer (329).

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After this weight loss tips for women generic alli 60mg without a prescription, the medial and dorsal aspects of the talonavicular joint weight loss pills 10 mg alli 60 mg sale, and the medial and lateral aspects of the subtalar joint are released. Both the talonavicular and subtalar joints are then pinned in a reduced position, and if needed the extensor and peroneal tendons can be lengthened. B: After serial casting, patient underwent open talonavicular pin fixation and percutaneous tenotomy of the Achilles tendon. A,B: K-wire placed into posterolateral aspect of talus and used as joystick to elevate talus into reduced position while plantarflexing the navicular and forefoot. Calcaneus deformity occurs in approximately 30% of patients with myelomeningocele. It is most common in patients with L4 or L5 level of involvement due to strength or spasticity of the ankle dorsiflexors combined with weakness of plantar flexion (31, 34, 124). Calcaneovalgus results from imbalance between the ankle evertors and the invertors. When the deformity is rigid, it can be very difficult to treat conservatively or surgically. If left untreated, calcaneus deformity causes loss of normal toe-off and a crouch gait (31, 124). Persistent weight bearing on a calcaneus deformity leads to a bulbous heel prone to pressure sores and secondary osteomyelitis (31). External tibia torsion frequently develops in association with calcaneovalgus but can be avoided by early correction of the muscle imbalance (17). Surgical treatment with anterolateral release including tenotomy of all ankle dorsiflexors and the peroneus brevis and longus can achieve a plantigrade, braceable foot. Rodrigues and Dias (125) reported a series of 76 patients treated with anterolateral release and achieved a good result in 82%. The poor results were due to either recurrence requiring a second release or equinus deformity requiring release of the Achilles tendon. The authors have found the anterolateral release to be a simpler procedure than the anterior tibial tendon transfer to the os calcis with similar results. They noted no recurrence or worsening of the deformity in any patient and no other type of foot deformity developed after the surgery. In older patients who have developed significant bony deformity, surgical correction requires not only release of all the extensor tendons and peroneals if needed, but also bony correction. A closing wedge osteotomy of the calcaneus with a plantar release can improve hindfoot alignment. If calcaneal valgus is present, a lateral opening wedge osteotomy of the cuboid may be necessary to achieve complete correction. Valgus deformities of the hindfoot and ankle are common in ambulatory patients with myelomeningocele. Successful treatment depends on identifying the precise anatomical location of the deformity that can arise from the distal tibia, hindfoot, or both. Valgus deformities tend to become more pronounced as a child matures, begins ambulation, and gains weight (114). Often as the hindfoot progresses into more valgus, skin irritation and breakdown over the medial malleolus and talar head result from excessive pressure against the brace. Surgery is indicated for severe, rigid deformities causing pain, difficulty with brace wear, or ulceration (114). Treatment options include distal tibia osteotomy, hemiepiphyseodesis of the distal tibia, or medial displacement osteotomy of the calcaneus. Hemiepiphysiodesis is indicated for mild deformities with sufficient growth remaining. Temporary growth arrest of the medial physis with continued growth of the lateral physis allows gradual correction of the valgus tilt. Use of a single cannulated screw has been reported in a series of 50 ft with satisfactory improvement of ankle valgus, low morbidity, and no incidence of permanent physeal closure (126). To avoid permanent closure of the physis, the screw should be removed within 2 years of its insertion.

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Segmental spinal dysgenesis: report of four cases and proposed management strategy weight loss pills meridian order 60 mg alli fast delivery. Sacral agenesis: a clinical evaluation of its management weight loss running buy alli 60 mg, heredity, and associated anomalies. Partial and complete agenesis or malformation of the sacrum with associated anomalies. Prevalence, concordance, and heritability of Scheuermann kyphosis based on a study of twins. Results of surgical treatment by posterior spine arthrodesis in twentytwo patients. Idiopathic scoliosis in three dimensions: a radiographic and morphometric analysis. Part I: development of a reliable and sensitive measure of disability in low-back pain. Nonoperative treatment of adolescent hyperkyphosis: a 30 years experience in over 3000 treated patients. Combined anterior-posterior fusion with laterally placed threaded interbody c ages and pedicle screws for Scheuermann kyphosis. Correction of adolescent hyperkyphosis with posterior-only threaded rod compression instrumentation: is anterior spinal fusion still necessary? Analysis of cervical instability resulting from laminectomies for removal of spinal cord tumor. Analysis and prevention of spinal column deformity following cervical laminectomy I. Spinal sagittal malalignment following surgery for primary intramedullary tumours in children. Spinal column deformity and instability after lumbar or thoracolumbar laminectomy for intraspinal tumors in children and young adults. Postlaminoplasty kyphotic deformity in the thoracic spine: case report and review of the literature. Incidence of spinal deformity in children after multiple level laminectomy for selective posterior rhizotomy. Combined laminoplasty and posterolateral fusion for spinal canal surgery in children and adolescents. Spinal deformity following surgery for spinal cord tumors and tumorous lesions: analysis based on an assessment of spinal functional curve. Swan-neck deformity following extensive cervical laminectomy: a review of twenty one cases. Cervical spinal deformity following craniotomy and upper cervical laminectomy for posterior fossa tumors in children. Skeletal effects of ortho-voltage and megavoltage therapy following treatment of nephroblastoma. Spinal deformity induced by radiotherapy for solid tumors in childhood: a long-term followup study. Postlaminectomy kyphosis in an achondroplastic adolescent treated for spinal stenosis. The beaked, notched or hooked vertebra: its significance in infants and young children. The Marfan syndrome locus: confirmation of assignment to chromosome 15 and identification of tightly-linked markers at 15 q 15-921. Iatrogenic kyphosis: a complication of Harrington instrumentation in Marfan syndrome. Scoliosis in Marfan syndrome: its characteristics and results of treatment in thirty-five patients. Thoracic lordoscoliosis in Marfan syndrome: report of two patients with surgical correction using rods and sublaminar wires. A new symptom-complex consisting of deafness, dwarfism, cleft palate, characteristic facies, and generalized bone dysplasia.

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The incision should be a straight line between these two points so that the scar lies in the midline and will be nearly straight after correction of the curve weight loss pills 2x purchase alli 60mg. If weight loss 90 purchase alli 60mg visa, however, the curve is severe and the correction is not anticipated to approach 30 degrees, the incision can be made in a curved manner following the shape of the deformity. After a slight cut partly through the dermis, the tissues can be infiltrated with a solution of adrenaline and saline (1:500,000). The needle follows the spinous process down to the lamina (B), and 5 mL of the same solution is injected at each level and on each side. It is important to identify and stay in the midline so that muscle is not cut, with consequent bleeding. The midline is identified by a thin line, which is actually the interspinous ligaments connecting the spinous processes. In severe cases of scoliosis with marked rotation, the muscles on the concave side are rolled up and over the midline, requiring that the knife (or cautery tip) be angled under it to reach the midline. After the apophysis of each spinous process is identified, it is split down to the bone with a knife or a cautery. The spinous process of the lamina above the one to be instrumented is exposed by pulling the cartilaginous tip of the spinous process off (A), turning the elevator with flat surface against the spinous process and sliding it down in the direction of the spinous process onto the lamina and the base of the transverse process. Care should be taken to follow the direction of the spinous process to avoid entering muscle and also to prevent unnecessary bleeding. This procedure is then performed on the vertebra below so that the spinous process, the lamina, and the base of the transverse process of that vertebra are stripped of periosteum. These structures, however, are obscured by the muscle tissue on top of the elevator. The attachment of this muscle (B) to the caudal edge of the more superior lamina (the first one exposed) is not obvious. The cut starts laterally or medially, but it should go from the tip of the spinous process to the lateral edge of the facet joint (dotted line). Division of these attachments is aided by placing the tissue under tension with the elevator. After the cut has been completed and the loose fatty tissue cleared from between the spinous processes, the elevator is placed in the cut that was made over the facet joint (A). From here, the elevator is drawn up the cephalad aspect of the transverse process (B). The very tip of the transverse process is obscured by the ligamentous attachment to the rib and, in most circumstances, can be left undisturbed provided that sufficient bone is exposed. Before repeating these steps on the next vertebra, it is important to expose carefully the caudal edge of the vertebra just cleaned. With a small twisting motion of the elevator, the periosteum is cleared until the rounded edge of the bone can be seen. If this is not accomplished, it will not be possible to view the facet clearly to cut the capsule, and the result will be shreds of soft tissue remaining on the bone. If a curette is used to remove the soft tissue from the facet joints, it should be used in a lateral-to-medial direction to avoid inadvertent penetration of the ligamentum flavum and possible spinal cord injury. In the lumbar spine the anatomy is different, and therefore, the technique is different. The space between these processes is filled with a thick ligament that cannot be divided as easily as in the thoracic spine. Using the elevator to place the tissues under tension, this ligament is divided by cutting between the two spinous processes (A). Although the anatomy appears different in this region, the principles are the same. Because the ligamentous attachments are on the caudal edge of the more cephalad lamina (B), they are divided sharply as the elevator applies tension and continues the subperiosteal dissection of the lamina. The easiest way to expose the facet joint is to follow the lamina out to the point where there is no more bone. Proceeding in a cranial direction from here is the inferior articular process, which in turn leads to the inferior facet. With the inferior articular process and the capsule of the facet exposed, a knife or an electrocautery is used to divide the capsule, starting on the inferior articular process and going in a cranial direction across the facet capsule (dotted line).

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For example weight loss programs alli 60 mg free shipping, 30 degrees of kyphosis is normal in the thoracic spine but abnormal at the thoracolumbar junction weight loss pills cheap effective generic 60mg alli free shipping. The normal range of thoracic kyphosis is considered to be 19 to 45 degrees and that of lumbar lordosis, 30 to 60 degrees (9). Measurements of kyphosis and lordosis are made from standard scoliosis radiographs with the patient standing with his or her knees locked, feet shoulder width apart, elbows bent, and knuckles in the supraclavicular fossa bilaterally. Thoracic kyphosis is measured on a lateral radiograph as the angle between the superior end plate of T2 and the inferior end plate of T12. Proximal thoracic kyphosis is measured from the superior end plate of T2 to the inferior end plate of T5. Middle and lower thoracic kyphosis is measured from the superior end plate of T5 to the inferior end plate of T12. Lumbar lordosis begins at L1Ό2 and increases gradually until the L3Ό4 disc space. A sacral slope of <35 degrees and a low pelvic incidence are associated with a relatively flat, short lumbar lordosis. A sacral slope of more than 45 degrees and a high pelvic incidence are associated with a long, curved lumbar lordosis (14). Initially, during fetal and intrauterine development, the entire spine is kyphotic. During the neonatal period, the thoracic, lumbar, and sacral portions of the spine remain in a kyphotic posture. Cervical lordosis begins to develop when a child starts holding his or her head up. When an upright posture is assumed, the primary and secondary curves begin to develop. The primary curves are thoracic and sacral kyphosis, and the secondary or compensatory curves in the sagittal plane are cervical and lumbar lordosis. These curves balance each other so that the head is centered over the pelvis (2, 17, 18). The ranges of normal thoracic kyphosis and lumbar lordosis are dynamic, progressing gradually with growth (19). During the juvenile and adolescent growth periods, thoracic kyphosis and lumbar lordosis become more pronounced and take on a more adult appearance. Differences also exist between male and female spines (6), and thoracic kyphosis and spine mobility are different in boys and girls: during the juvenile and adolescent periods (ages 8 to 16 years), girls have less thoracic kyphosis and thoracic spinal mobility than do boys of the same age (3, 12). Thoracic kyphosis also tends to progress with age: from 30 to 70 years of age, women have a progressive increase in kyphosis, from a mean of 25 degrees to a mean of 40 degrees (19). Radiographic measurements of pelvic incidence (a), sacral slope (b), and pelvic tilt (c). A plumb line is dropped from the middle of the C7 vertebral body to the posterosuperior corner of the S1 vertebral body. Positive sagittal balance occurs when the plumb line falls in front of the sacrum, and negative sagittal balance occurs when the plumb line falls behind the sacrum (20). Different forces are exerted on the spine, depending on the presence of kyphosis or lordosis. In the upright position, the spine is subjected to the forces of gravity, and several structures maintain its stability: the disc complex (nucleus pulposus and annulus), the ligaments (anterior longitudinal ligament, posterior longitudinal ligament, ligamentum flavum, apophyseal joint ligaments, and interspinous ligament), and the muscles (the long spinal muscles, the short intrinsic spinal muscles, and the abdominal muscles). Alteration in function resulting from paralysis, surgery, tumor, infection, or alteration in growth potentials can cause a progressive kyphotic deformity in a child (21). In normal thoracic kyphosis, the compressive forces borne by the anterior elements are balanced by the tensile forces borne by the posterior elements. In a lordotic spine, the compressive forces are posterior and the tensile forces are anterior. These forces of compression and tension on the spinal physes can cause changes in normal growth, and a growth deformity can be added to a biomechanical deformity to cause a pathologic kyphosis (21, 22). Voutsinas and MacEwen (23) suggested that relative differences in forces applied to the spine are reflected more accurately by the length and width of a kyphotic curve than by just the degree of the curve. Postural kyphosis should be differentiated from pathologic types of kyphosis, such as Scheuermann disease, and from congenital kyphosis. Patients with Scheuermann disease and congenital kyphosis have a sharp angular kyphosis or gibbus on forward bending when observed from the side. Patients with postural kyphosis do not have radiographic vertebral-body changes, and the deformity is completely correctable by changes in position or posture.

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Several tissue cultures should be sent during surgery before antibiotics are administered weight loss pills garcinia cambogia gnc cheap alli uk. Sending specimens to pathology for microscopic examination may also be helpful in establishing a diagnosis size 0 weight loss pills purchase generic alli from india, especially if all cultures turn out to be negative. There have been several recent reports of successful arthroscopic joint debridement for septic arthritis of the knee, hip, and shoulder (144, 145, 169ͱ71). The specific joint involved, chronicity of the infection, experience of the surgeon, and experience of the allied health staff available at the time of surgery should be considered before deciding to perform arthroscopic joint debridement. In the hands of an experienced arthroscopist, debridement of relatively inaccessible areas such as the posterior compartment of the knee can be performed, and the joint can be irrigated with a very large volume of fluid. One distinct disadvantage of arthroscopic debridement is that because the arthroscope is looking out from the inside of the joint, it may be very difficult to accurately assess the depth of the purulent material and the extent of infection, especially in chronic cases. Most recently, in a randomized prospective study of culture positive acute septic arthritis in children, Peltola et al. The patient is positioned supine with a generous bump placed beneath the affected hemipelvis to elevate the hemipelvis and hip 30 to 45 degrees from the table. Prepping and draping the entire leg and buttocks into the surgical field allows full movement of the hip intraoperatively to thoroughly dꣲide and irrigate the hip. The incision, placed about a finger breadth beneath the anterosuperior iliac spine, can be transverse or oblique and can be smaller than an incision used for other major hip procedures because it is not necessary to expose the outer table of the ilium. The interval between the sartorius and the tensor muscles is identified and separated up to the anterosuperior iliac spine. If necessary, the periosteum can be elevated from the outer table of the ilium in the region of the anterosuperior iliac spine; however, after some experience with this approach, this step is usually not required. At the base of the exposure between the sartorius and the tensor muscles is the rectus femoris muscle. In this area, close to the anteroinferior iliac spine, its tendinous portion can be identified. A periosteal elevator can be used to separate the fatty tissue covering this tendon. The lateral border of this tendon with its muscular origin is freed and retracted medially. It is covered by the precapsular fatty tissue, which may be thick and edematous in the septic hip. This can also be separated with a periosteal elevator, scissors, or scalpel to expose the hip capsule, and the capsule is then incised. A cruciate incision has been used with good effect, but the author prefers to excise a window of capsule to allow free and unhindered drainage. Whether a cruciate incision or a capsular window is used, care must be exercised to incise the capsule over the anterior femoral neck and the base of the femoral head, avoiding vessels that supply the epiphysis as they ascend along the superior aspect of the femoral neck. Total treatment duration of approximately 3 weeks is appropriate, depending on clinical and laboratory response to treatment. Parenteral antibiotics should be initiated, with conversion to oral antibiotics after favorable clinical response for total treatment duration of approximately 3 weeks, depending on clinical and laboratory response to treatment. Chronic hematogenous osteomyelitis: When symptoms have been present for more than 3 weeks, in association with bone abscess or destruction, surgical debridement is indicated. Tissue cultures are obtained at surgery, and depending on culture results, extent of infection, and response to treatment, a long-term course of parenteral antibiotics for 6 to 8 weeks is often appropriate. Bone grafting or bone transport may be used to fill large bone defects and can be performed 3 to 4 weeks after initiating parenteral antibiotic treatment. A small red rubber catheter, with multiple perforations cut into the tip, may be passed around the femoral neck and into the various recesses of the joint to provide thorough irrigation. Inspection should ensure that no fibrinous clots of inflammatory material remain in the joint. After complete irrigation and debridement, a drainage catheter is place inside the hip joint, exiting the patient percutaneously through the hip abductors and the skin anterolaterally. The muscles are allowed to fall back together and the deep fascia and skin are closed.

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Occasionally an excisional biopsy weight loss rewards purchase alli 60mg on-line, rather than an incisional biopsy weight loss pills herbal buy alli with mastercard, is indicated. Open excisional biopsy differs from incisional biopsy in that the entire tumor is excised and sent for analysis. An excisional biopsy is appropriate when the lesion is small and can be excised with a cuff of normal tissue. If the preoperative evaluation strongly supports the diagnosis of a malignancy, particularly one for which a frozen section analysis will be difficult to do, an excisional biopsy should be considered. The advantages include single surgical procedure; however, a significant disadvantage is the need for extensive tissue sacrifice if re-excision is necessary (malignant tumor) to obtain appropriate margins. An added advantage of an excisional biopsy is that the pathologist is able to examine the entire lesion, thereby improving the accuracy of the pathologic examination. An incisional biopsy exposes uncontaminated tissues to the tumor, and if the tumor proves to be a malignancy, the definitive resection is more complicated. If the lesion can be treated with curettage or a marginal excision, the incisional biopsy leads to the least functional loss. Some patients want to take the fewest chances, and are willing to accept the possibility of slight overtreatment, whereas others choose to take one step at a time. A final note of caution is offered with regard to the biopsy: osteomyelitis is more common than bone tumors, especially in children, and osteomyelitis often mimics neoplasia. This 14-year-old girl had an unplanned excision of a "lipoma" of the dorsum of her foot, performed at an outside institution (A). The patient needed re-excision of the lesion with oncologic margins (B) and the soft-tissue defect created needed skin grafting (C). The authors have tried to confine the discussion to pertinent information regarding the tumors, their evaluation, and particularly their treatment. Osteoid osteoma is a benign active bone tumor that accounts for 11% of the benign bone tumors in Dahlin series from the Mayo Clinic (73). Osteoid osteoma most commonly affects boys (3:1 girl) between 5 and 24 years of age (80% of all patients). McLeod (74) is credited with the initial description, distinguishing it from a Brodie abscess, and from Garre osteomyelitis. If a patient has the typical pain for an osteoid osteoma, but there is no relief by aspirin, the diagnosis should be doubted. Patients with osteoid osteoma show few abnormalities on physical examination, with the exception of scoliosis in patients with osteoid osteoma of the spine. Although osteoid osteomas may arise in any bone, around 50% are found in the femur and tibia. The usual radiographic appearance is one of dense reactive bone with new bone periosteal formation, the actual lesion (a. The nidus may be on the surface of the bone, within the cortex, or on the endosteal surface. When a child presents with painful scoliosis, with or without atypical curve pattern, osteoid osteoma should be considered (75ͷ7). A technetium-99 bone scan is particularly useful to localize the lesion otherwise missed on the plain radiograph (78). Note the intracortical lytic (nidus) lesion, surrounded by new bone formation, no periosteal reaction or soft-tissue mass (arrow). On gross inspection, the nidus of an osteoid osteoma is cherry-red and surrounded by dense white bone. A lesion that is identical histologically to the nidus of an osteoid osteoma, but larger than 2 cm, is called an osteoblastoma. Natural history shows that osteoid osteoma may heal spontaneously although that may take several years (75, 80). This is a 13-year-old boy with lower neck pain, worse at night and torticollis; anteriorΰosterior (A) radiographs of the cervical spine is not diagnostic and only shows malalignment due to muscle spasm.

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Comparative study of Fanconi anemia in children of different ethnic origin in South Africa weight loss pills 74 best 60mg alli. The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry weight loss pills appetite suppressant alli 60 mg mastercard. Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry. Dysplasia of the knee associated with the syndrome of thrombocytopenia and absent radius. Lower extremity deformities associated with thrombocytopenia and absent radius syndrome. Arms and the man or hands and the child: congenital anomalies and hematologic syndromes. Diagnosing and treating Diamond Blackfan anemia: results of an International Clinical Consensus Conference. Gene transfer improves erythroid development in ribosomal protein S19-deficient Diamond-Blackfan anemia. Hematopoietic stem cell transplantation for bone marrow failure syndromes in children. Anemia in children with cartilage-hair hypoplasia is related to body growth and to the insulin-like growth factor system. Bone marrow transplantation in cartilage-hair hypoplasia: correction of the immuno-deficiency but not of the chondrodysplasia. Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin. Septicemia caused by Salmonella infection: an overlooked complication of sickle cell disease [Comment]. Clinical events in the first decade in a cohort of infants with sickle cell disease. Salmonella osteomyelitis and hand-foot syndrome in a child with sickle cell anemia. Retrospective review of osteoarticular infections in a pediatric sickle cell age group. Differentiation between bone infarction and acute osteomyelitis in children with sickle-cell disease with use of sequential radionuclide bone-marrow and bone scans. The natural history of untreated asymptomatic osteonecrosis of the femoral head: a systematic literature review. The natural history of asymptomatic osteonecrosis of the femoral head in adults with sickle cell disease. Risk factors for osteonecrosis of the femoral head in patients with sickle cell disease. Deformities of the hip in adults who have sickle-cell disease and had avascular necrosis in childhood. Physical therapy alone compared with core decompression and physical therapy for femoral head osteonecrosis in sickle cell disease. The value of ultrasound and aspiration in differentiating vaso-occlusive crisis and osteomyelitis in sickle cell disease patients. The perioperative complication rate of orthopedic surgery in sickle cell disease: report of the National Sickle Cell Surgery Study Group. Use of the tourniquet during surgery in patients with sickle cell hemoglobinopathies. Pathological fracture complicating long bone osteomyelitis in patients with sickle cell disease. Prophylactic antibiotics for preventing pneumococcal infection in children with sickle cell disease. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia [Comment]. Extraordinary intrathecal bone reaction in beta-thalassaemia intermedia [Comment]. Spinal cord compression secondary to extramedullary hematopoiesis in thalassemia intermedia. Short stature and failure of pubertal development in thalassaemia major: evidence for hypothalamic neurosecretory dysfunction of growth hormone secretion and defective pituitary gonadotropin secretion.