A familial syndrome of cranial, facial, oral and limb anomalies
- 1 October 1976
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 10 (4) , 226-231
- https://doi.org/10.1111/j.1399-0004.1976.tb00039.x
Abstract
A family is described in which 2 male infants have microcephaly, abnormal ears, antimongoloid slant, small mouth, cleft palate, flexed overlapping fingers with syndactyly of the 3rd and 4th digits, syndactyly of the 2nd to 5th toes and normal karyotype. This seems to be a new syndrome.This publication has 5 references indexed in Scilit:
- Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.Journal of Medical Genetics, 1968
- TRISOMY-E-LIKE SYNDROMEThe Lancet, 1965
- Trisomy-18 Syndrome in a Patient With Normal KaryotypePublished by American Medical Association (AMA) ,1965
- Chromosome 18: A topologic approachThe Journal of Pediatrics, 1965
- Clinical Trisomy E Syndrome (16-18)Clinical Pediatrics, 1964