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A familial syndrome of cranial, facial, oral and limb anomalies
Author(s) -
Fitch Naomi,
Jequier Sigrid,
Papageorgiou Apostolos
Publication year - 1976
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.1399-0004.1976.tb00039.x
Subject(s) - syndactyly , microcephaly , medicine , anatomy , ectrodactyly , pediatrics , dermatology , ectodermal dysplasia
A family is described in which two male infants have microcephaly, abnormal ears, anti‐mongoloid slant, small mouth, cleft palate, flexed overlapping fingers with syndactyly of digits three and four, syndactyly of the second to the fifth toes, and normal karyotype. This seems to be a new syndrome.