| Literature DB >> 28247548 |
S Khalil1, R Hayashi2, L Daou3, S A Staiteieh4, O Abbas5, C Bergqvist5, G Nemer4, Y Shimomura2,6, M Kurban4,5,7.
Abstract
The Wnt signalling pathway is a major pathway involved in the embryogenic development of the various organs of the body. Appropriate signalling in this pathway relies on the proper functioning of several proteins including the R-spondin family of proteins. Deactivating mutations in R-spondin 4 are associated with anonychia. We present the case of a 26-year-old man presenting with anonychia of the 20 nails, which had been present since birth. Using genetic studies, we identified a novel nonsense mutation, c.164-165TC>AA, characterized by two consecutive mismatch bases. To our knowledge, this mutation is the first to be reported in R-spondin 4 in a Lebanese population. Evaluating new patients with anonychia provides fruitful clinical and molecular findings.Entities:
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Year: 2017 PMID: 28247548 DOI: 10.1111/ced.13052
Source DB: PubMed Journal: Clin Exp Dermatol ISSN: 0307-6938 Impact factor: 3.470