Unknown diagnosis in two male cousins with facial abnormalities, optic atrophy, abnormal EEG, and severe psychomotor retardation
Author: Mégarbané A
Source:
American Journal of Medical Genetics Part A, 116(4), 381-384.
We report two male cousins with short stature, microcephaly, hypertelorism, optic
atrophy, ptosis, absent ear lobes, high-arched palates, abnormal EEG, and severe
mental retardation. Both cousins have consanguineous parents. Differential
diagnoses are discussed and the possibility that we might be reporting on a new
syndrome is raised. Copyright 2003 Wiley-Liss, Inc