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Article
November 1980

Long-Limbed Campomelic Dwarfism: A Radiologic and Pathologic Study

Author Affiliations

From the Departments of Pathology (Drs Austin, Mirra, and Perry), Radiology (Dr Gold), and Medical Genetics (Dr Moedjono), UCLA School of Medicine. Dr Austin is now with the Emory University Hospital, Atlanta.

Am J Dis Child. 1980;134(11):1035-1042. doi:10.1001/archpedi.1980.02130230015005
Abstract

• Comparison of the roentgenographic and pathologic features of a case of classic, long-limbed campomelic dwarfism with those of previously reported cases leads to the conclusion that the bony abnormalities in this disorder are not due to an intrinsic abnormality of cartilage formation or of osteoblast or osteoclast function. Likewise, no defect in bone collagen, ground substance, or mineralization is evident. The bowing of the long bones may be the result of poorly understood muscular stresses operative in utero. Widespread defects in other organ systems are present, with considerable variation from patient to patient. Phenotypic females with the disorder commonly suffer from gonadal dysgenesis. Autosomal recessive inheritance is suggested for a subgroup of these patients, but environmental factors may be causative in some instances.

(Am J Dis Child 134:1035-1042, 1980)

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