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Article

Ichthyosis with confetti presenting as collodion baby: a novel mutation in KRT10.

Clinical and experimental dermatology - 1 Jul 2017

Foo S H, Terron-Kwiatkowski A, Baty D, Browne F

Abstract excerpt

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Share to Ichthyosiform Erythroderma, Congenital
Share to Ichthyosis, Lamellar
Share to Infant, Newborn
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 28556375
DOI: 10.1111/ced.13097

Genes

KRT10

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

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Ichthyosis with confetti presenting as collodion baby: a novel mutation in KRT10.PMID 28556375Read ↗

The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3' end of KRT10: from disease to a syndrome.Semantic proximity Read ↗

Ichthyosis with confetti: clinics, molecular genetics and management.Semantic proximity Read ↗

Expanding the Mutation Spectrum of Ichthyosis with Confetti.Semantic proximity Read ↗

Case of ichthyosis with confetti caused by KRT10 mutation, complicated with multiple malignant melanomas.Semantic proximity Read ↗

Genotype-phenotype correlations with TGM1: clustering of mutations in the bathing suit ichthyosis and self-healing collodion baby variants of lamellar ichthyosis.Semantic proximity Read ↗

Description of the natural course and clinical manifestations of ichthyosis with confetti caused by a novel KRT10 mutation.Semantic proximity Read ↗

Ichthyosis with Confetti Inherited from a Mosaic Father.Semantic proximity Read ↗

A case of epidermolytic ichthyosis showing a very mild phenotype due to a novel tail extension mutation in KRT10.Semantic proximity Read ↗

Phenotypic variation in epidermolytic ichthyosis: clinical and functional evaluation of the novel p.(Met339Lys) mutation in the L12 domain of KRT1.Semantic proximity Read ↗

Lamellar ichthyosis in a collodion baby caused by CYP4F22 mutations in a non-consanguineous family outside the Mediterranean.Semantic proximity Read ↗

A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene.Semantic proximity Read ↗

Coexistence of mutations in keratin 10 (KRT10) and the mitochondrial genome in a patient with ichthyosis with confetti and Leber's hereditary optic neuropathy.Semantic proximity Read ↗

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