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These case reports discuss a novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association
Abstract:
Mutations of the PTEN gene are associated with hamartoma-neoplasia syndromes. While germline mutations at this chromosome 10q22-23 locus have been observed in patients with Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRR), both of which phenotypes are associated with hamartomata and neoplasia, somatic mutation of PTEN has been established in a wide variety of more...
International Classification:
Syndrome V.A.T.E.R. syndrome Vertebrae, Anus, Trachea, Esophagus, and Renal
Categories:
V.A.T.E.R. syndrome - abnormalities: Vertebrae, Anus, Trachea, Esophagus, and Renal
Geography:
Republic of Ireland
J Med Genet,
Vol: 38 Page: 820-3 December 2001
W. Reardon; X. P. Zhou; C. Eng
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