Cutis Laxa Latest Advances

Find the Latest Research About Cutis Laxa

Last Updated: 04/28/2026

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Found 1027 publications

Cutis Laxa and Basilar Predominant Emphysema.

Cutis Laxa and Basilar Predominant Emphysema.

Journal: Radiology. Cardiothoracic imaging

Published: January 08, 2026

Idiopathic Localized Acquired Cutis Laxa in an Adult Male: A Case Report.

Idiopathic Localized Acquired Cutis Laxa in an Adult Male: A Case Report.

Journal: Cureus

Published: January 02, 2026

Cutis laxa associated with a missense variant in elastin gene.

Cutis laxa associated with a missense variant in elastin gene.

Journal: JAAD case reports

Published: December 26, 2025

Cutis laxa syndrome with ascending aortic aneurysm in a child: Bentall procedure and subsequent interventional rescue.

Cutis laxa syndrome with ascending aortic aneurysm in a child: Bentall procedure and subsequent interventional rescue.

Journal: Cardiology in the young

Published: December 22, 2025

Monoclonal Gammopathies of Cutaneous Significance (MGCS): A Nomenclature and Pathophysiology Based Classification.

Monoclonal Gammopathies of Cutaneous Significance (MGCS): A Nomenclature and Pathophysiology Based Classification.

Journal: Journal of the American Academy of Dermatology

Published: November 06, 2025

ATP6V0A2-Related Cutis Laxa: Identification of a Recurrent Exon 16 Deletion With Founder Effect in Southeastern Türkiye and a Novel Frameshift Variant.

ATP6V0A2-Related Cutis Laxa: Identification of a Recurrent Exon 16 Deletion With Founder Effect in Southeastern Türkiye and a Novel Frameshift Variant.

Journal: American journal of medical genetics. Part A

Published: October 22, 2025

Classical complement activation in light and heavy chain deposition disease with acquired cutis laxa and bronchiolitis obliterans: a case report of monoclonal gammopathy of clinical significance.

Classical complement activation in light and heavy chain deposition disease with acquired cutis laxa and bronchiolitis obliterans: a case report of monoclonal gammopathy of clinical significance.

Journal: Frontiers in immunology

Published: October 06, 2025

Novel POLR3A Gene Mutation Results in Wiedemann-Rautenstrauch Syndrome With Striking Cutis Laxa and Myelofibrosis.

Novel POLR3A Gene Mutation Results in Wiedemann-Rautenstrauch Syndrome With Striking Cutis Laxa and Myelofibrosis.

Journal: The Journal of dermatology

Published: September 29, 2025

Beyond the genome: a rare case report of cutis laxa.

Beyond the genome: a rare case report of cutis laxa.

Journal: AME case reports

Published: September 22, 2025

Cutis Laxa Type 1 B with Recurrent E57K Variation.

Cutis Laxa Type 1 B with Recurrent E57K Variation.

Journal: Indian journal of dermatology

Published: September 08, 2025

Genes associated with genetic and rare lung diseases and the risk of lung cancer.

Genes associated with genetic and rare lung diseases and the risk of lung cancer.

Journal: Research square

Published: August 20, 2025

Abnormal von Willebrand factor multimer pattern without VWF variants in autosomal-recessive cutis laxa type IIA.

Abnormal von Willebrand factor multimer pattern without VWF variants in autosomal-recessive cutis laxa type IIA.

Journal: Blood vessels, thrombosis & hemostasis

Published: August 12, 2025

Showing 1-12 of 1,027

Last Updated: 04/28/2026