Peeling Skin Syndrome Latest Advances

Deletion of the Epidermal Protease KLK5 Aggravates the Symptoms of Congenital Ichthyosis CDSN-nEDD.

Journal: International journal of molecular sciences

Published: August 04, 2025

Genetic profiling of epidermolysis bullosa in a large Brazilian cohort.

Journal: Clinical and experimental dermatology

Published: March 07, 2025

Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients.

Journal: Pediatric dermatology

Published: October 28, 2024

Coincidence of acral peeling skin syndrome and Nagashima-type palmoplantar keratosis in a Japanese pedigree with acral skin peeling.

Journal: The Journal of dermatology

Published: May 23, 2024

A case of peeling skin syndrome type 1 with novel CDSN gene variation successfully treated with upadacitinib.

Journal: The Journal of dermatology

Published: April 24, 2024

Variants in the L12 linker domain of KRT10 are causal to atypical epidermolytic ichthyosis.

Journal: The Journal of dermatology

Published: March 14, 2024

Acral Peeling Skin Syndrome: Two Unusual Cases and the Therapeutic Potential of Botulinum Toxin.

Journal: Acta dermato-venereologica

Published: October 25, 2023

Staphylococcal Scalded Skin Syndrome, Identification, and Wound Care: A Case Report Series.

Journal: Advances in neonatal care : official journal of the National Association of Neonatal Nurses

Published: July 28, 2022

Correction to: Peeling Skin Syndrome Type 1: Dupilumab Reduces IgE, But Not Skin Anomalies.

Journal: Journal of clinical immunology

Published: July 23, 2022

A patient with PLACK syndrome with a novel splicing mutation in CAST: the evidence for a loss-of-function mechanism through mis-splicing.

Journal: Clinical and experimental dermatology

Published: July 09, 2022

Atopic Dermatitis-like Genodermatosis: Disease Diagnosis and Management.

Journal: Diagnostics (Basel, Switzerland)

Published: May 30, 2022

A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata.

Journal: Pediatric dermatology

Published: February 18, 2022

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Deletion of the Epidermal Protease KLK5 Aggravates the Symptoms of Congenital Ichthyosis CDSN-nEDD.

Deletion of the Epidermal Protease KLK5 Aggravates the Symptoms of Congenital Ichthyosis CDSN-nEDD.

Genetic profiling of epidermolysis bullosa in a large Brazilian cohort.

Genetic profiling of epidermolysis bullosa in a large Brazilian cohort.

Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients.

Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients.

Coincidence of acral peeling skin syndrome and Nagashima-type palmoplantar keratosis in a Japanese pedigree with acral skin peeling.

Coincidence of acral peeling skin syndrome and Nagashima-type palmoplantar keratosis in a Japanese pedigree with acral skin peeling.

A case of peeling skin syndrome type 1 with novel CDSN gene variation successfully treated with upadacitinib.

A case of peeling skin syndrome type 1 with novel CDSN gene variation successfully treated with upadacitinib.

Variants in the L12 linker domain of KRT10 are causal to atypical epidermolytic ichthyosis.

Variants in the L12 linker domain of KRT10 are causal to atypical epidermolytic ichthyosis.

Acral Peeling Skin Syndrome: Two Unusual Cases and the Therapeutic Potential of Botulinum Toxin.

Acral Peeling Skin Syndrome: Two Unusual Cases and the Therapeutic Potential of Botulinum Toxin.

Staphylococcal Scalded Skin Syndrome, Identification, and Wound Care: A Case Report Series.

Staphylococcal Scalded Skin Syndrome, Identification, and Wound Care: A Case Report Series.

Correction to: Peeling Skin Syndrome Type 1: Dupilumab Reduces IgE, But Not Skin Anomalies.

Correction to: Peeling Skin Syndrome Type 1: Dupilumab Reduces IgE, But Not Skin Anomalies.

A patient with PLACK syndrome with a novel splicing mutation in CAST: the evidence for a loss-of-function mechanism through mis-splicing.

A patient with PLACK syndrome with a novel splicing mutation in CAST: the evidence for a loss-of-function mechanism through mis-splicing.

Atopic Dermatitis-like Genodermatosis: Disease Diagnosis and Management.

Atopic Dermatitis-like Genodermatosis: Disease Diagnosis and Management.

A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata.

A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata.