GUADALAJARA CAMPTODACTYLY SYNDROME - A DISTINCT PROBABLY AUTOSOMAL RECESSIVE DISORDER
- 1 January 1980
- journal article
- research article
- Vol. 18 (3) , 153-159
Abstract
Two sisters, aged 18 and 11 yr, had intrauterine growth retardation-malformation syndrome which included camptodactyly as a typical sign. The overall analysis of the clinical and radiological findings permitted the individualization of a distinct entity. The family data suggested autosomal recessive inheritance.This publication has 2 references indexed in Scilit:
- OCULODENTODIGITAL DYSPLASIA SYNDROME Report of Four CasesActa Paediatrica, 1977
- Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome.Journal of Medical Genetics, 1976