Piebaldism with café‐au‐lait macules resulting from a novel mutation of KIT gene in a three‐generation Chinese family

Abstract

AbstractBackgroundPiebaldism is a rare, autosomal dominant, and congenital pigmentary disorder characterized by stable depigmentation of the skin and white forelock. Mutations in KIT or SLUG genes result in piebaldism. Most individuals with piebaldism have a family history of the disorder.MethodsIn this paper, we report a case of piebaldism with café‐au‐lait macules resulting from a novel mutation of KIT gene c.1982C > T (p.Thr661Ile) in a three‐generation Chinese family. The whole‐exome sequencing, mitochondrial gene 3000X, and bioinformatics tools were used to identify the mutation in this new‐found pedigree. In addition, we searched the databases of “Punmed, Chinese National Knowledge Infrastructure, CMJD, WANFANG MED ONLINE”, reviewed 88 cases of piebaldism caused by KIT gene mutation, and summarized the relationship between clinical phenotype and genotype of piebaldism through logistic regression and other statistical methods.ResultsThe proband and her affected mother carried a heterozygous c.1982C > T missense mutation (p.Thr661Ile) on KIT gene. Bioinformatics analysis hinted that it had potential pathogenicity. The data showed that piebaldism patients with cafè‐au‐lait macules had KIT mutations almost located in the intracellular tyrosine kinase domain and were mostly related to the severe clinical phenotype of piebaldism.ConclusionThe new heterozygous c.1982C > T missense mutation on KIT caused piebaldism with café‐au‐lait macules in this Chinese family. This study provides a new reference index for clinicians to judge the severity of clinical phenotypes of piebaldism, broadens the understanding of the correlation between clinical phenotypes and genotypes of piebaldism, and provides reference of genetic counseling and prenatal diagnosis for affected families.