Langer type of mesomelic dwarfism as the possible homozygous expression of dyschondrosteosis |
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Authors: | J. P. Fryns H. Van Den Berghe |
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Affiliation: | (1) Division of Human Genetics, Department of Human Biology, Minderbroedersstraat, 12, B-3000 Leuven, Belgium |
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Abstract: | Summary A male newborn with the typical Langer type of mesomelic dwarfism is presented. The finding of a variable degree of Madelung's deformity and mesomelic shortening in both parents and in the maternal family tends to support the hypothesis that this type of mesomelic dwarfism may be the clinical manifestation of a homozygous state for dyschondrosteosis. |
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