| Literature DB >> 15889419 |
Paul A James1, Paul Oei, Daniel Ng, Peter Kannu, Salim Aftimos.
Abstract
Recent reports of patients with interstitial deletions involving the long arm of chromosome 12 have led to the proposal of a candidate region for the cardio-facio-cutaneous syndrome (CFCS) at (12)(q21.2q22). We now report a patient with an interstitial deletion, del(12)(q21.1q21.3) that overlaps the proposed critical region. The patient is an 11-year-old female with developmental delay. Her growth was normal but she is microcephalic with low set ears. In common with other patients with deletions in this region, she had fine, sparse head and eyebrow hair and a hyperkeratotic follicular rash, which involved her face and limbs. She does not have the diagnostic features of the CFC syndrome. Copyright (c) 2005 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2005 PMID: 15889419 DOI: 10.1002/ajmg.a.30693
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802