Case Report: Contrasting outcomes and use of desmosine to monitor two patients treated with plasma cell-directed chemotherapy for gammopathy-driven pulmonary elastolysis in acquire... by Lydia Lee, Emma Fosbury, Rakesh Popat, Kwee Yong, Ashutosh Wechalekar, Jeremy S. Brown, Jeffrey Huang, Sandy Mcbride, John R. Hurst

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Blefaroplastia com cantopexia em paciente portadora de cútis laxa: Um relato de caso by JOSE ISNACK PONTE DE ALENCAR, JOSé ALBERTO GUILHERME FROTA-JúNIOR, GUILHERME PINHO CARDOSO, VITOR DE VASCONCELLOS MUNIZ, FERNANDO SOARES DE ALCâNTARA, SALUSTIANO GOMES DE PINHO PESSOA

Subjects: “…Cútis laxa…”
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Blepharoplasty with canthopexy in a patient with cutis laxa: A case report by Jose Isnack Ponte de Alencar, José Alberto Guilherme Frota-Júnior, Guilherme Pinho Cardoso, Vitor de Vasconcellos Muniz, Fernando Soares de Alcântara, Salustiano Gomes de Pinho Pessoa

Subjects: “…cutis laxa…”
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Case Report: de novo in-frame deletion in PLCG2 gene: a case report of B-cell lymphopenia, pulmonary bullae, and cutis laxa by Xiaoqi Wu, Xiaoqi Wu, Jingyuan Zhang, Jingyuan Zhang, Min Shen, Min Shen

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Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome by Mark T. Handley, André Mégarbané, Alison M. Meynert, Stephen Brown, Elisabeth Freyer, Martin S. Taylor, Ian J. Jackson, Irene A. Aligianis

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A Japanese Case of Lenz‐Majewski Syndrome With a Novel PTDSS1 Variant by Yasuko Kobari, Non Miyata, Jun Takayama, Naoya Saijo, Tomohisa Suzuki, Shigeo Kure, Atsuo Kikuchi, Gen Tamiya, Takumi Takizawa

Subjects: “…congenital cutis laxa…”
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A Shared Pathogenesis? Elastic Tissue Degeneration in Two Generations: Co‐Occurrence of Acrokeratoelastoidosis and ARCL1A Cutis Laxa by Sumayyah I Alrefaie, Sarah B. Aljoudi, Houriah Y. Nukaly, Waseem K. Alhawsawi, Asem Shadid, Sultan AlNasser, Jehad Hariri

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Corrigendum: Case report and literature review: delayed diagnosis of ARCL1B due to a newly reported homozygous mutation c.464A>C p. (Tyr155Ser) in the EFEMP2 gene by Lixue Ouyang, Lixue Ouyang, Lixue Ouyang, Fan Yang, Fan Yang, Hongyu Duan, Hongyu Duan, Chuan Wang, Chuan Wang, Chuan Wang

Subjects: “…autosomal recessive cutis laxa type 1B…”
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