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Murray Feingold, MD
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Reprint requests to Tufts—New England Medical Center, Boston Floating Hospital, 171 Harrison Ave, Boston, MA 02111 (Dr Feingold).


Am J Dis Child. 1984;138(5):503-504. doi:10.1001/archpedi.1984.02140430079021.
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Denouement and Discussion 

Hereditary Multiple Exostoses (Diaphyseal Aclasis) 

Manifestations  The exostoses are usually present by the age of 10 years but, on occasion, may be noted in infancy. They vary in size and location, with the most common sites being the scapula, ends of the long bones, ribs, and iliac crest. Following puberty, growth usually stops, and no new lesions appear. The exostoses can affect the growth of the long bones, resulting in various deformities, such as bowing of the radius, shortening of the ulna, radiohumeral dislocation, genu valgum, and valgus deformities of the ankles. Other skeletal abnormalities include scoliosis, short stature, and thoracic and pelvic deformities. Malignant degeneration of the exostoses (chondrosarcomas) takes place in approximately 5% to 10% of the patients. They are usually diagnosed in the early 30s age group, and most often are located in the pelvis and the femur. On roentgenographic examination, the exostoses are

REFERENCES

Solomon L:  Hereditary multiple exostoses . Am J Hum Genet 1964;;16:351.
Solomon L:  Chondrosarcoma in hereditary multiple exostoses . S Afr Med J 1974;;48:671-676.
Shapiro F, Simon S, Glimcher MJ:  Hereditary multiple exostoses: Anthropometric, roentgenographic, and clinical aspects . J Bone Joint Surg Am 1979;;61:815-824.

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Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

Use interactive graphics and maps to view and sort country-specific infant and early dhildhood mortality and growth failure data and their association with maternal

References

Solomon L:  Hereditary multiple exostoses . Am J Hum Genet 1964;;16:351.
Solomon L:  Chondrosarcoma in hereditary multiple exostoses . S Afr Med J 1974;;48:671-676.
Shapiro F, Simon S, Glimcher MJ:  Hereditary multiple exostoses: Anthropometric, roentgenographic, and clinical aspects . J Bone Joint Surg Am 1979;;61:815-824.

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