| Literature DB >> 26851524 |
Kornélia Tripolszki1, Rachel Knox2, Victoria Parker2, Robert Semple2, Katalin Farkas3, Adrien Sulák1, Emese Horváth1, Márta Széll4, Nikoletta Nagy5.
Abstract
Isolated macrodactyly (OMIM 155500) belongs to a heterogeneous group of overgrowth syndromes. It is a congenital anomaly resulting in enlargement of all tissues localized to the terminal portions of a limb and caused by somatic mutations in the phosphatidylinositol 3-kinase catalytic alpha (PIK3CA, OMIM 171834) gene. Here we report a Hungarian girl with macrodactyly and syndactyly. Genetic screening at hotspots in the PIK3CA gene identified a mosaic mutation (c.1624G > A, p.Glu542Lys) in the affected tissue, but not in the peripheral blood. To date, this somatic mutation has been reported in eight patients affected by different forms of segmental overgrowth syndromes. Detailed analysis of the Hungarian child and previously reported cases suggests high phenotypic diversity associated with the p.Glu542Lys somatic mutation. The identification of the mutation provides a novel therapeutic modality for the affected patients: those who carry somatic mutations in the PIK3CA gene are potential recipients of a novel "repurposing" approach of rapamycin treatment.Entities:
Keywords: Macrodactyly and syndactyly; Overgrowth syndromes; PIK3CA gene; Phenotypic diversity; Somatic mutation
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Year: 2016 PMID: 26851524 DOI: 10.1016/j.ejmg.2016.02.002
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708