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Guadalajara camptodactyly syndrome
Author(s) -
Cantú J. M.,
Rivera H.,
Nazará Z.,
Rojas Q.,
Hernández A.,
GarcíaCruz D.
Publication year - 1980
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1980.tb00863.x
Subject(s) - camptodactyly , medicine , pediatrics , genetics , biology , anatomy
Two sisters, aged 18 and 11 years, were found to have an intrauterine growth retardaion‐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.