| Literature DB >> 8275567 |
L E Figuera1, D García-Cruz, M L Ramírez-Dueñas, V Rivera-Robles, J M Cantù.
Abstract
Two unrelated Mexican girls, aged 14 months and 6 years respectively, with Kaufman oculocerebrofacial syndrome, are reported. Both showed psychomotor retardation, microcephaly, blepharophimosis and delayed growth as the main features; the infant also presented preauricular tags and large clitoris. Comparative analysis with previous cases reveals a heterogeneous syndrome in which the micro-brachycephaly, the mongoloid slanted eyes with different anomalies, the micrognathia and the neonatal respiratory distress are the most typical characteristics of this mental retardation syndrome.Entities:
Mesh:
Year: 1993 PMID: 8275567 DOI: 10.1111/j.1399-0004.1993.tb03855.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438