Erythrokeratodermia Variabilis et Progressiva Latest Advances

Find the Latest Research About Erythrokeratodermia Variabilis et Progressiva

Last Updated: 06/30/2026

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Found 190 publications

Establishment of spinocerebellar ataxia type 34 model mice accompanied by early glial activation and degeneration of cerebellar neurons.

Establishment of spinocerebellar ataxia type 34 model mice accompanied by early glial activation and degeneration of cerebellar neurons.

Journal: Journal of pharmacological sciences
Published: February 10, 2026

A Pediatric Case of KRT2 Nonsyndromic Epidermal Differentiation Disorder With a Concurrent GJB4 Variant.

A Pediatric Case of KRT2 Nonsyndromic Epidermal Differentiation Disorder With a Concurrent GJB4 Variant.

Journal: The Journal of dermatology
Published: October 06, 2025

Erythrokeratodermia Variabilis et Progressiva 4 With KDSR Mutations: A Case Report.

Erythrokeratodermia Variabilis et Progressiva 4 With KDSR Mutations: A Case Report.

Journal: The Journal of dermatology
Published: August 16, 2025

Recessive mosaicism in ABCA12 causes a unique phenotype of segmental congenital ichthyosiform erythroderma mimicking erythrokeratodermia variabilis.

Recessive mosaicism in ABCA12 causes a unique phenotype of segmental congenital ichthyosiform erythroderma mimicking erythrokeratodermia variabilis.

Journal: Dermatology reports
Published: March 10, 2025

Erythrokeratodermia Variabilis et Progressiva With Compound Heterozygous ABCA12 Variants.

Erythrokeratodermia Variabilis et Progressiva With Compound Heterozygous ABCA12 Variants.

Journal: The Australasian journal of dermatology
Published: January 30, 2025

Nonsyndromic epidermal differentiation disorders: a new classification toward pathogenesis-based therapy.

Nonsyndromic epidermal differentiation disorders: a new classification toward pathogenesis-based therapy.

Journal: The British journal of dermatology
Published: November 05, 2024

A novel missense mutation responsible for a patient with unique erythrokeratodermia variabilis with skin lesions in a swirling pattern.

A novel missense mutation responsible for a patient with unique erythrokeratodermia variabilis with skin lesions in a swirling pattern.

Journal: Clinical and experimental dermatology
Published: October 10, 2024

Adult-onset erythrokeratodermia variabilis (EKV) triggered by pregnancy and crash dieting: A rare case report.

Adult-onset erythrokeratodermia variabilis (EKV) triggered by pregnancy and crash dieting: A rare case report.

Journal: JPMA. The Journal of the Pakistan Medical Association
Published: September 16, 2024

Protean cutaneous manifestation caused by ABCA12 variants: erythrokeratodermia variabilis-like ichthyosis and unique palmoplantar keratoderma.

Protean cutaneous manifestation caused by ABCA12 variants: erythrokeratodermia variabilis-like ichthyosis and unique palmoplantar keratoderma.

Journal: Clinical and experimental dermatology
Published: August 16, 2024

Erythrokeratodermia Variabilis due to a Compound Heterozygous Variants in the NIPAL4 Gene.

Erythrokeratodermia Variabilis due to a Compound Heterozygous Variants in the NIPAL4 Gene.

Journal: Pediatric dermatology
Published: July 17, 2024

The genetic and molecular basis of a connexin-linked skin disease.

The genetic and molecular basis of a connexin-linked skin disease.

Journal: The Biochemical journal
Published: July 15, 2024

Skin disease-associated GJB4 variants differentially influence connexin stability, cell viability and channel function.

Skin disease-associated GJB4 variants differentially influence connexin stability, cell viability and channel function.

Journal: The Journal of physiology
Published: June 04, 2024
Showing 1-12 of 190

Last Updated: 06/30/2026