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Am J Med Genet. 1991 May 1;39(2):170-2.

Unique dwarfing, spondylometaphyseal skeletal dysplasia, with joint laxity and dentinogenesis imperfecta.

Author information

1
Department of Genetics, Princess Margaret Hospital for Children, Perth, Western Australia.

Abstract

We report a 3 1/2-year-old boy with a unique spondylometaphyseal dysplasia with predominantly mesomelic involvement. In addition, he had gross generalised joint laxity and dentinogenesis imperfecta.

PMID:
2063920
DOI:
10.1002/ajmg.1320390211
[Indexed for MEDLINE]

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