Lamellar Ichthyosis Latest Advances

Find the Latest Research About Lamellar Ichthyosis

Last Updated: 02/24/2026

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Found 1302 publications

Harlequin Ichthyosis in a Preterm Neonate: A Case Report.

Harlequin Ichthyosis in a Preterm Neonate: A Case Report.

Journal: Cureus
Published: November 27, 2025

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.

Journal: Cureus
Published: November 15, 2025

Lamellar Ichthyosis Improvement With Acitretin and Dupilumab.

Lamellar Ichthyosis Improvement With Acitretin and Dupilumab.

Journal: JAMA dermatology
Published: October 22, 2025

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.

Journal: The Journal of international medical research
Published: October 08, 2025

ABCA12 Frameshift Deletion in Domestic Cats With Ichthyosis Fetalis.

ABCA12 Frameshift Deletion in Domestic Cats With Ichthyosis Fetalis.

Journal: Veterinary dermatology
Published: September 17, 2025

A Rare Familial Case of Harlequin Ichthyosis in an Infant of a Diabetic Mother: A Diagnostic and Management Challenge in Low and Middle Income Settings.

A Rare Familial Case of Harlequin Ichthyosis in an Infant of a Diabetic Mother: A Diagnostic and Management Challenge in Low and Middle Income Settings.

Journal: Clinical case reports
Published: July 28, 2025

Evaluation of the Efficacy of Transglutaminase 1 Gene Delivery by Adeno-Associated Virus into Rat and Pig Skin and Safety of ARCI Gene Therapy.

Evaluation of the Efficacy of Transglutaminase 1 Gene Delivery by Adeno-Associated Virus into Rat and Pig Skin and Safety of ARCI Gene Therapy.

Journal: International journal of molecular sciences
Published: July 23, 2025

Autosomal Recessive Congenital Ichthyosis Due to Heterozygote Variants in the ALOX12B gene Presenting as Mild Nonbullous Congenital Ichthyosiform Erythroderma.

Autosomal Recessive Congenital Ichthyosis Due to Heterozygote Variants in the ALOX12B gene Presenting as Mild Nonbullous Congenital Ichthyosiform Erythroderma.

Journal: Acta dermatovenerologica Croatica : ADC
Published: July 14, 2025

Beyond the skin: immunological profiles and infectious complications in ALOX12B-associated autosomal recessive congenital ichthyosis.

Beyond the skin: immunological profiles and infectious complications in ALOX12B-associated autosomal recessive congenital ichthyosis.

Journal: Frontiers in immunology
Published: July 09, 2025

"Fetal clues to Harlequin ichthyosis: Bridging sonography with genetic breakthroughs".

"Fetal clues to Harlequin ichthyosis: Bridging sonography with genetic breakthroughs".

Journal: Taiwanese journal of obstetrics & gynecology
Published: May 13, 2025

Expanding the clinical spectrum: A case report of the first Jordanian presentation of KID syndrome with neurological and skeletal anomalies beyond the classical triad.

Expanding the clinical spectrum: A case report of the first Jordanian presentation of KID syndrome with neurological and skeletal anomalies beyond the classical triad.

Journal: Medicine
Published: May 07, 2025

A case report and literature review of self-improving collodion baby in the newborn.

A case report and literature review of self-improving collodion baby in the newborn.

Journal: Medicine
Published: April 07, 2025
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Last Updated: 02/24/2026