| Literature DB >> 15258833 |
Naoki Harada1,2,3, Remco Visser1,4,5, Angie Dawson6, Makoto Fukamachi7, Mie Iwakoshi8, Nobuhiko Okamoto9, Tatsuya Kishino2,10, Norio Niikawa1,2, Naomichi Matsumoto11,12,13.
Abstract
Patients with 9q34.3 terminal deletion usually show a clinically recognizable phenotype characterized by specific facial features (microcephaly, flat face, arched eyebrows, hypertelorism, short nose, anteverted nostrils, carp mouth and protruding tongue) in combination with severe mental retardation, hypotonia, and other anomalies. We analyzed six unrelated patients with a various 9q34.3 terminal deletion. While having different-sized 9q34.3 deletions, all of these patients shared several distinctive anomalies. These anomalies are likely to arise from a commonly deleted region at distal 9q34.3. Fluorescence in situ hybridization (FISH) analysis using a dozen BAC clones mapped at the 9q34.13-q34.3 region defined the shortest region of deletion overlap (SRO) as a 1-Mb segment proximal to 9qter containing eight known genes. Possible candidate genes delineating specific phenotypes of the 9q34.3 terminal deletion syndrome are discussed.Entities:
Mesh:
Year: 2004 PMID: 15258833 DOI: 10.1007/s10038-004-0166-z
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172