| Literature DB >> 20658556 |
André Mégarbané1, Nathalie Dorison, Diana Rodriguez, Jean Tamraz.
Abstract
We report on two sibs with an elongated face with reduced expression, microcephaly, strabismus, wide philtrum, mild joint laxity, thumb sign, bilateral foot drop, and fixed pes cavus, absent tendinous reflexes, an unsteady gait, quick fatigue, slightly diminished limb muscle strength more pronounced distally, abnormalities of cranial nerves III, IV, VII, and most probably VI, and slowness in ideation. Previously unknown findings referred to as the "fork sign" at the pontine level and the "bracket sign" at the mesencephalic level were documented by magnetic resonance imaging. Differential diagnoses and the possibility of a hitherto unreported syndrome are discussed. Copyright 2010 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2010 PMID: 20658556 DOI: 10.1002/ajmg.a.33417
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802