A somatic PIK3CA p.H1047L mutation in a Thai patient with isolated macrodactyly: a case report

Author:

Udomchaiprasertkul Wandee1234,Kitidumrongsook Pravit5,Suphapeetiporn Kanya12,Shotelersuk Vorasuk12

Affiliation:

1. Center of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University , Bangkok 10330 , Thailand

2. Excellence Center for Genomics and Precision Medicine, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society , Bangkok 10330 , Thailand

3. Interdisciplinary Program of Biomedical Sciences, Graduate School, Chulalongkorn University , Bangkok 10330 , Thailand

4. Molecular Biology and Genomic Research Laboratory, Division of Research and International Relations, HRH Princess Chulabhorn College of Medical Science, Chulabhorn Royal Academy , Bangkok 10900 , Thailand

5. Department of Orthopedics, Faculty of Medicine, Chiang Mai University , Chiang Mai 50200 , Thailand

Abstract

Abstract Background Macrodactyly is a rare congenital deformity characterized by gigantism of all structures of the digits. Previous reports showed that the mosaic PIK3CA variants were associated with overgrowth syndromes including macrodactyly. Objectives To determine the genetic alteration in a Thai patient with enlarged soft tissue of the left middle and left fourth fingers with abnormal enlarged phalanges. Method A nerve and a skin piece were separated from a therapeutically surgically removed part of the enlarged digit. Skin fibroblasts were cultured from the removed skin piece. DNA was isolated from the nerve tissue, cultured skin fibroblasts, and peripheral blood leukocytes. Polymerase chain reaction (PCR) followed by Sanger sequencing of PIK3CA was performed. Results Mutation analysis revealed the c.3140A>T (p.(H1047L)) variant of PIK3CA in the nerve tissue and the cultured dermal fibroblasts but not in leukocytes from the peripheral blood. Conclusion The somatic c.3140A>T (p.(H1047L)) variant of PIK3CA was found in a Thai patient with isolated macrodactyly, the same as those previously identified in other populations.

Publisher

Walter de Gruyter GmbH

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