[CITATION][C] Unique dwarfing, spondylometaphyseal skeletal dysplasia, with joint laxity and dentinogenesis imperfecta
J Goldblatt, P Carman… - American journal of …, 1991 - Wiley Online Library
J Goldblatt, P Carman, P Sprague
American journal of medical genetics, 1991•Wiley Online LibraryUnique dwarfing, spondylometaphyseal skeletal dysplasia, with joint laxity and dentinogenesis
imperfecta Page 1 American Journal of Medical Genetics 39:170-172 (1991) Unique Dwarfing,
Spondylometaphyseal Skeletal Dysplasia, With Joint Laxity and Dentinogenesis Imperfecta
Jack Goldblatt, Paul Carman, and Paul Sprague Departments of Genetics (JG), Paediatrics
(PC) and Radiology (PS), Princess Margaret Hospital for Children, Perth, Western Australia
We report a 3%-year-old boy with a unique spondylometaphyseal dysplasia with …
imperfecta Page 1 American Journal of Medical Genetics 39:170-172 (1991) Unique Dwarfing,
Spondylometaphyseal Skeletal Dysplasia, With Joint Laxity and Dentinogenesis Imperfecta
Jack Goldblatt, Paul Carman, and Paul Sprague Departments of Genetics (JG), Paediatrics
(PC) and Radiology (PS), Princess Margaret Hospital for Children, Perth, Western Australia
We report a 3%-year-old boy with a unique spondylometaphyseal dysplasia with …
Abstract
We report a 3½‐year‐old boy with a unique spondylometaphyseal dysplasia with predominantly mesomelic involvement. In addition, he had gross generalised joint laxity and dentinogenesis imperfecta.
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