Cutis Laxa Latest Advances
Find the Latest Research About Cutis Laxa
Last Updated: 06/30/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 1035 publications
Two cases of lethal neonatal-type cutis laxa syndrome with sublingual outgrowths by homozygous variation of LTBP4 gene
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: June 16, 2026
Autosomal Dominant Cutis Laxa in an Adolescent Male: A Rare Clinical Entity.
Journal: Cureus
Published: April 04, 2026
Gelsolin amyloidosis presenting with nephrotic syndrome: a case report and molecular insights.
Journal: Frontiers in medicine
Published: January 29, 2026
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.
Journal: Cureus
Published: January 02, 2026
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.
Journal: Cardiology in the young
Published: December 22, 2025
Monoclonal gammopathies of cutaneous significance: 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.
Journal: American journal of medical genetics. Part A
Published: October 22, 2025
Acquired Cutis Laxa Secondary to Hematological Malignancy: A Report of Two Cases.
Journal: Indian dermatology online journal
Published: October 06, 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.
Journal: Frontiers in immunology
Published: October 06, 2025
Novel POLR3A Gene Mutation Results in Wiedemann-Rautenstrauch Syndrome With Striking Cutis Laxa and Myelofibrosis.
Journal: The Journal of dermatology
Published: September 29, 2025
Last Updated: 06/30/2026