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Article

Cohen syndrome coincident with epidermolytic palmoplantar keratoderma caused by novel KRT9 gene mutation: A rare case report.

Asian journal of surgery - 1 Dec 2023

Shu Yanping, Hou Yongzhe, Zhang Qin

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Identifiers

PMID: 37690893
DOI: 10.1016/j.asjsur.2023.08.206

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Related research

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Research trail→

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Cohen syndrome coincident with epidermolytic palmoplantar keratoderma caused by novel KRT9 gene mutation: A rare case report.PMID 37690893Read ↗

The common KRT9 gene mutation in a Japanese patient with epidermolytic palmoplantar keratoderma and knuckle pad-like keratoses.Semantic proximity Read ↗

Epidermolytic palmoplantar keratoderma of Vörner: re-evaluation of Vörner's original family and identification of a novel keratin 9 mutationSemantic proximity Read ↗

Nagashima-Type Palmoplantar Keratosis: Clinical Characteristics, Genetic Characterization, and Clinical Management.Semantic proximity Read ↗

Nonsense mutations in KRT1 caused recessive epidermolytic palmoplantar keratoderma with knuckle pads.Semantic proximity Read ↗

Epidermolytic hyperkeratosis with palmoplantar keratoderma in a patient with KRT10 mutation.Semantic proximity Read ↗

Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene.Semantic proximity Read ↗

Hereditary Palmoplantar KeratodermasSemantic proximity Read ↗

A novel mutation of keratin 9 in a large Chinese family with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

Palmoplantar keratodermas: clinical and genetic aspects.Semantic proximity Read ↗

[Present status of the molecular genetics in epidermolytic palmoplantar keratoderma].Semantic proximity Read ↗

A unique case of palmoplantar keratoderma.Semantic proximity Read ↗

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