Disease: Cutis laxa
- <em>ATP6V0A2</em>-Related Cutis Laxa
- <em>EFEMP2</em>-Related Cutis Laxa
- <em>FBLN5</em>-Related Cutis Laxa
- <em>FBLN5</em>-Related Cutis Laxa Syndrome: A Case with a Novel Variant and Review of the Literature
- <em>LTBP4</em>-Related Cutis Laxa
- A case of cutis verticis gyrata developing in a patient with primary scarring alopecia: A unique presentation of a rare disorder
- A case of monoclonal gammopathy of cutaneous significance with multiple organs involvement: Comment on "Concurrent acquired cutis laxa and necrobiotic xanthogranuloma without paraproteinemia"
- A Growth-Restricted Neonate with Abnormal Facies and Lax Skin
- A novel intronic variant of ATP6V0A2-related cutis laxa with impaired cognitive function
- A rare case of secondary cutaneous lymphoplasmacytic lymphoma clinically presenting as acquired cutis laxa
- Acquired cutis laxa secondary to acute generalized exanthematous pustulosis: A case report and mini-review of literature
- Acquired cutis laxa: a clinical review
- Atlantoaxial instability associated with ALDH18A1 mutation
- ATP6V1A variants are associated with childhood epilepsy with favorable outcome
- Characterization of the Zebrafish <em>Elastin a</em> (<em>elna<sup>sa12235</sup></em>) Mutant: A New Model of Elastinopathy Leading to Heart Valve Defects
- Clinical features in adults with acquired cutis laxa: a retrospective review
- Comprehensive review of aortic aneurysms, dissections, and cardiovascular complications in connective tissue disorders
- Concurrent acquired cutis laxa and necrobiotic xanthogranuloma without paraproteinemia
- Confirming the enzymatic activity and neurodevelopmental trajectory of PYCR1 mutation in one child with autosomal-recessive cutis laxa type 2
- Corkscrew Mesenteric Arteries and Tortuous Descending Aorta in Autosomal Recessive Cutis Laxa
- Cutis Laxa
- Cutis Laxa and the Value of Rhytidectomy: 4 Patients and Years of Follow-Up
- Deep intronic variant causes aberrant splicing of ATP7A in a family with a variable occipital horn syndrome phenotype
- Discovery of pathogenic variants in EFEMP2 and RAG1 and undetectable fetal phenotype: A challenge of prenatal exome sequencing
- Dynamic Reconstruction Using Bilateral Lengthening Temporalis Myoplasty for Facial Palsies in Patients with Hereditary Skin Laxity
- Effect of decreased expression of latent TGF-β binding proteins 4 on the pathogenesis of emphysema as an age-related disease
- Expanding the phenotype and metabolic basis of ATP6AP2-congenital disorder of glycosylation in a Chinese patient with a novel variant c.185G>A (p.Gly62Glu)
- Extreme arterial tortuosity with ascending aortic aneurysm in a child with suspected Cutis Laxa syndrome
- Free Dermal Fat Grafting: A Novel Technique for the Correction of Nasolabial Folds During Facelift Surgery
- Giant ascending aortic aneurysm with impending rupture as presentation of cutis laxa 1B: a case report
- Identification of a novel intronic variant of ATP6V0A2 in a Han-Chinese family with cutis laxa
- Lenz-Majewski syndrome and recurrent otitis media: Are they related or not?
- Neonatal presentation of occipital horn syndrome caused by a ATP7A missense variant
- Novel mutation in ELN gene causes cardiac abnormalities and inguinal hernia: case report
- Penicillamine-Induced Localised Cutis Laxa in a Patient with Wilson Disease: A Case Report
- Progressive Generalized Skin Laxity in a Young Woman
- Severe atopic dermatitis with cutis laxa caused by a variant in the ELN gene
- Surgical Management of Hip Dislocation in a Patient with SCARF Syndrome: A Case Report with a 6-Year Follow-up
- The Human Mutation K237_V238del in a Putative Lipid Binding Motif within the V-ATPase a2 Isoform Suggests a Molecular Mechanism Underlying Cutis Laxa
- Two novel homozygous variants of ATP6V0A2 and ALDH18A1 lead to autosomal recessive cutis laxa type 2 and 3 in two Pakistani families
- Type I acquired cutis laxa: Report of a unique progressive case and short review
- Type I acquired cutis laxa: report of a unique progressive case. A short review
- Visceral adiposity in patients with lipomatous hypertrophy of the interatrial septum
- Wells syndrome and acquired cutis laxa: An atypical association