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Spondylometaphyseal dysplasia in two sibs of normal parents.

作者信息

Gustavson K H, Holmgren G, Probst F

出版信息

Pediatr Radiol. 1978 Jun 19;7(2):90-6. doi: 10.1007/BF00975677.

Abstract

Two sibs with identical features of short-limbed dwarfism, a normal skull and face and normal intelligence are described. On the basis of the radiological and clinical characteristics the condition must be included within the group of spondylometaphyseal dysplasias. In contrast to the familial cases described up to now in which the mode of inheritance was autosomal dominant, the trait in the two children described here was transmitted as an autosomal recessive.

摘要

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