Nonbullous Congenital Ichthyosiform Erythroderma Latest Advances

Characterizing superficial epidermolytic ichthyosis in a patient with KRT2 mutation responsive to ustekinumab.

Journal: JAAD case reports

Published: March 05, 2026

Phenotypic and genotypic analysis of five fetuses with Harlequin ichthyosis due to variants of ABCA12 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: February 06, 2026

Hypopigmented lesions admixed with verrucous papules in a child with epidermolytic verrucous epidermal nevus.

Journal: BMJ case reports

Published: January 06, 2026

Lamellar Ichthyosis in a Resource-Limited Setting: A Somaliland Case Report.

Journal: International medical case reports journal

Published: December 01, 2025

Harlequin Ichthyosis in a Preterm Neonate: A Case Report.

Journal: Cureus

Published: November 27, 2025

From variant of unknown significance to actionable diagnosis: Stepwise interpretation of a novel KRT2 variant in superficial epidermolytic ichthyosis with excellent retinoid response.

Journal: JAAD international

Published: November 17, 2025

Ichthyosis Prematurity Syndrome Caused by a Novel Homozygous SLC27A4 Mutation in Two Emirati Siblings.

Journal: Cureus

Published: November 15, 2025

Pediatric Lamellar Ichthyosis.

Journal: Paediatric anaesthesia

Published: November 06, 2025

Neonatal Erythroderma: Diagnostic Challenges and the Limitations of Genetic Testing.

Journal: Cureus

Published: November 04, 2025

Lamellar Ichthyosis Improvement With Acitretin and Dupilumab.

Journal: JAMA dermatology

Published: October 22, 2025

Identification of Novel Mutation in the ABCA12 Gene Causing Harlequin Ichthyosis.

Journal: Clinical case reports

Published: October 12, 2025

A novel mutation in the transglutaminase-1 gene identified in a collodion baby: A case report.

Journal: The Journal of international medical research

Published: October 08, 2025

Nonbullous Congenital Ichthyosiform Erythroderma Latest Advances

Find the Latest Research About Nonbullous Congenital Ichthyosiform Erythroderma

Characterizing superficial epidermolytic ichthyosis in a patient with KRT2 mutation responsive to ustekinumab.

Characterizing superficial epidermolytic ichthyosis in a patient with KRT2 mutation responsive to ustekinumab.

Phenotypic and genotypic analysis of five fetuses with Harlequin ichthyosis due to variants of ABCA12 gene

Phenotypic and genotypic analysis of five fetuses with Harlequin ichthyosis due to variants of ABCA12 gene

Hypopigmented lesions admixed with verrucous papules in a child with epidermolytic verrucous epidermal nevus.

Hypopigmented lesions admixed with verrucous papules in a child with epidermolytic verrucous epidermal nevus.

Lamellar Ichthyosis in a Resource-Limited Setting: A Somaliland Case Report.

Lamellar Ichthyosis in a Resource-Limited Setting: A Somaliland Case Report.

Harlequin Ichthyosis in a Preterm Neonate: A Case Report.

Harlequin Ichthyosis in a Preterm Neonate: A Case Report.

From variant of unknown significance to actionable diagnosis: Stepwise interpretation of a novel KRT2 variant in superficial epidermolytic ichthyosis with excellent retinoid response.

From variant of unknown significance to actionable diagnosis: Stepwise interpretation of a novel KRT2 variant in superficial epidermolytic ichthyosis with excellent retinoid response.

Ichthyosis Prematurity Syndrome Caused by a Novel Homozygous SLC27A4 Mutation in Two Emirati Siblings.

Ichthyosis Prematurity Syndrome Caused by a Novel Homozygous SLC27A4 Mutation in Two Emirati Siblings.

Pediatric Lamellar Ichthyosis.

Pediatric Lamellar Ichthyosis.

Neonatal Erythroderma: Diagnostic Challenges and the Limitations of Genetic Testing.

Neonatal Erythroderma: Diagnostic Challenges and the Limitations of Genetic Testing.

Lamellar Ichthyosis Improvement With Acitretin and Dupilumab.

Lamellar Ichthyosis Improvement With Acitretin and Dupilumab.

Identification of Novel Mutation in the ABCA12 Gene Causing Harlequin Ichthyosis.

Identification of Novel Mutation in the ABCA12 Gene Causing Harlequin Ichthyosis.

A novel mutation in the transglutaminase-1 gene identified in a collodion baby: A case report.

A novel mutation in the transglutaminase-1 gene identified in a collodion baby: A case report.