Ahmad, Farooq, Nasir, Abdul ORCID: 0000-0002-2339-3500, Thiele, Holger, Umair, Muhammad, Borck, Guntram and Ahmad, Wasim (2018). A novel homozygous missense variant in NECTIN4 (PVRL4) causing ectodermal dysplasia cutaneous syndactyly syndrome. Ann. Hum. Genet., 82 (4). S. 232 - 239. HOBOKEN: WILEY. ISSN 1469-1809

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Abstract

Ectodermal dysplasia syndactyly syndrome 1 (EDSS1) is a rare form of ectodermal dysplasia including anomalies of hair, nails, and teeth along with bilateral cutaneous syndactyly of hands and feet. In the present report, we performed a clinical and genetic characterization of a consanguineous Pakistani family with four individuals affected by EDSS1. We performed exome sequencing using DNA of one affected individual. Exome data analysis identified a novel homozygous missense variant (c.242T>C; p.(Leu81Pro)) in NECTIN4 (PVRL4). Sanger sequencing validated this variant and confirmed its cosegregation with the disease phenotype in the family members. Thus, our report adds a novel variant to the NECTIN4 mutation spectrum and contributes to the NECTIN4-related clinical characterization.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Ahmad, FarooqUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nasir, AbdulUNSPECIFIEDorcid.org/0000-0002-2339-3500UNSPECIFIED
Thiele, HolgerUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Umair, MuhammadUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Borck, GuntramUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Ahmad, WasimUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-182305
DOI: 10.1111/ahg.12244
Journal or Publication Title: Ann. Hum. Genet.
Volume: 82
Number: 4
Page Range: S. 232 - 239
Date: 2018
Publisher: WILEY
Place of Publication: HOBOKEN
ISSN: 1469-1809
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
CELL-CELL ADHESION; MUTATIONS; AFADIN; RAC1; GENE; FAMILY; EDSS1Multiple languages
Genetics & HeredityMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/18230

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