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Article

Congenital monilethrix and hereditary unilateral external auditory canal atresia are co-inherited in a Chinese pedigree with recurrent KRT86 mutation.

The Journal of dermatology - 1 Sept 2012

Feng Yi-Guo, Xiao Sheng-Xiang, Xu Ai-Li, Feng Jin-Yun, Wang Jun-Min

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Identifiers

PMID: 22568869
DOI: 10.1111/j.1346-8138.2012.01565.x

Genes

KRT86

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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Congenital monilethrix and hereditary unilateral external auditory canal atresia are co-inherited in a Chinese pedigree with recurrent KRT86 mutation.PMID 22568869Read ↗

Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family.Semantic proximity Read ↗

Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene.Semantic proximity Read ↗

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A recurrent missense mutation in the KRT16 gene causing pachyonychia congenita in a patient.Semantic proximity Read ↗

Mutation E402K of the hHb6 in a Chinese Han family with monilethrix.Semantic proximity Read ↗

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A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin.Semantic proximity Read ↗

Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families.Semantic proximity Read ↗

Association of external auditory canal atresia, vertical talus, and hypertelorism: confirmation of Rasmussen syndrome.Semantic proximity Read ↗

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