| Literature DB >> 9321771 |
A Mégarbané1, N Souraty, M Prieur, D Theophile, P Chédid, J Augé, M Vekemans.
Abstract
An 18 month old girl was referred to us because of dysmorphic features and psychomotor and growth retardation. On physical examination, she was found to have microcephaly, open fontanelles, a prominent forehead, a flat occiput, hypertelorism, sparse eyebrows, a small nose with a depressed nasal bridge, a bulging philtrum, a thin upper lip, a high arched palate, low set and posteriorly rotated ears, a small mandible, a short neck with a low hair line, and eye malformations. High resolution chromosome analysis identified a de novo direct duplication of the 2p21.00-->p24.2 region. The phenotype of de novo partial trisomy 2p is discussed.Entities:
Mesh:
Year: 1997 PMID: 9321771 PMCID: PMC1051069 DOI: 10.1136/jmg.34.9.783
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318