Works matching DE "CUTIS laxa"

Results: 124

Generalized granulomatous slack skin.

Published in:

British Journal of Dermatology, 2025, v. 192, n. 6, p. 1148, doi. 10.1093/bjd/ljae508

By:

Chen, Zirui;
Wang, Yang;
Wang, Ruojun

Publication type:

Article

Giant ascending aortic aneurysm with impending rupture as presentation of cutis laxa 1B: a case report.

Published in:

European Heart Journal Case Reports, 2023, v. 7, n. 11, p. 1, doi. 10.1093/ehjcr/ytad530

By:

Used-Gavín, Alejandro;
Larrañaga-Moreira, José María;
Lago-Cascudo, Rafael;
Mosquera-Rodríguez, Víctor X;
Barriales-Villa, Roberto

Publication type:

Article

Anaesthetic Management in a Child with Cutis Laxa for Bilateral Ureteric Reimplantation.

Published in:

Archives of Anesthesiology & Critical Care, 2021, v. 7, n. 3, p. 176

By:

Ramachandran, Haripriya;
Bhagya, Dammaningala Venkataramaiah

Publication type:

Article

Clinical commentary about foreign body complications over 20 years after polymethyl‐methacrylate face implants and control of late sequelae with Polynucleotides Highly Purified Technology (PN‐HPT<sup>®</sup>).

Published in:

Journal of Cosmetic Dermatology, 2022, v. 21, n. 11, p. 5537, doi. 10.1111/jocd.14950

By:

Palmieri, Isabella Pia;
Raichi, Mauro

Publication type:

Article

Chronic urticaria may not be as innocent as we think: A rare case of acquired cutis laxa following chronic urticaria.

Published in:

2022

By:

Bostan, Ecem;
Yalici‐Armagan, Basak;
Gokoz, Ozay

Publication type:

Case Study

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.

Published in:

Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 4, p. 319, doi. 10.1002/mgg3.70

By:

Handley, Mark T.;
Mégarbané, André;
Meynert, Alison M.;
Brown, Stephen;
Freyer, Elisabeth;
Taylor, Martin S.;
Jackson, Ian J.;
Aligianis, Irene A.

Publication type:

Article

Autosomal-dominant cutis laxa resulting from an intronic mutation in ELN.

Published in:

2015

By:

Vodo, Dan;
Sarig, Ofer;
Peled, Alon;
Frydman, Moshe;
Greenberger, Shoshi;
Sprecher, Eli

Publication type:

Case Study

The complexity of elastic fibre biogenesis in the skin - a perspective to the clinical heterogeneity of cutis laxa.

Published in:

Experimental Dermatology, 2013, v. 22, n. 2, p. 88, doi. 10.1111/exd.12025

By:

Uitto, Jouni;
Li, Qiaoli;
Urban, Zsolt

Publication type:

Article

The Histopathological Findings of Patients Who Underwent Blepharoplasty Due to Dermatochalasis.

Published in:

2018

By:

Karnaz, Ali;
Katircioglu, Yasemin Aslan;
Ozdemir, Evin Singar;
Celebli, Pınar;
Hucumenoglu, Sema;
Ornek, Firdevs

Publication type:

journal article

Acquired cutis laxa secondary to sweet syndrome (marshall syndrome) in a 2-year-old child.

Published in:

Indian Journal of Paediatric Dermatology, 2021, v. 22, n. 3, p. 254, doi. 10.4103/ijpd.IJPD_89_20

By:

Asha, Gowrappala;
Radhika, Seetharampura;
Shilpa, Kanathur;
Ramesh, Heera

Publication type:

Article

Acquired Cutis Laxa Secondary to Sweet Syndrome (Marshall Syndrome) in a 2-Year-Old Chil.

Published in:

Indian Journal of Paediatric Dermatology, 2021, v. 22, n. 1, p. 254, doi. 10.4103/ijpd.IJPD_89_20

By:

Asha, Gowrappala Shanmukhappa;
Radhika, Seetharampura Ramamurthy;
Shilpa, Kanathur;
Ramesh, Heera

Publication type:

Article

Autosomal recessive cutis laxa type-1 with complex systemic manifestations.

Published in:

Indian Journal of Paediatric Dermatology, 2018, v. 19, n. 3, p. 274, doi. 10.4103/ijpd.IJPD_65_17

By:

Chavan, Shruti;
Deshmukh, Ashish;
Gulanikar, Aniruddha;
Pathrikar, Shilpa;
Tariq, Iqbal

Publication type:

Article

Phenotypic overlap in autosomal recessive cutis laxa: Report of two siblings.

Published in:

2017

By:

Arif, Tasleem;
Nisa, Nuzhatun;
Rather, Shagufta;
Shah, Sheena

Publication type:

Letter to the Editor

Sweet's syndrome leading to acquired cutis laxa in a child (Marshall's syndrome): A rare case report.

Published in:

2016

By:

Bangaru, H.;
Surendran, K. A. K.;
Nanjundaswamy, B. L.;
Vijaya, B.

Publication type:

Case Study

Marshall’s syndrome.

Published in:

2016

By:

Meena, Neha;
Sharma, Prafulla K.;
Bhardwaj, Minakshi;
Kumar, Sawan

Publication type:

Case Study

Atypical Presentation of Gelsolin Amyloidosis in a Man of African Descent with a Novel Mutation in the Gelsolin Gene.

Published in:

2018

By:

Oregel, Karlos Z.;
Shouse, Geoffrey P.;
Oster, Cyrus;
Martinez, Freddy;
Jun Wang;
Rosenzweig, Michael;
Deisch, Jeremy K.;
Chien-Shing Chen;
Nagaraj, Gayathri

Publication type:

Case Study

Cutis laxa Case report.

Published in:

Archives of Hellenic Medicine / Arheia Ellenikes Iatrikes, 2017, v. 34, n. 2, p. 253

By:

Darban, B.;
Moradi, M.

Publication type:

Article

Neurofibromatosis Type 1-related Multiple Plexiform Neurofibromas: A Case Report.

Published in:

Turkish Journal of Neurology / Turk Noroloji Dergisi, 2020, v. 26, n. 1, p. 42, doi. 10.4274/tnd.2019.44520

By:

Bayram, Tamer;
Bayram, Derya;
Tireli, Hülya

Publication type:

Article

Extreme arterial tortuosity with ascending aortic aneurysm in a child with suspected Cutis Laxa syndrome.

Published in:

2025

By:

Singh, Damandeep;
Pandey, Niraj Nirmal;
Gupta, Saurabh Kumar;
Jagia, Priya

Publication type:

Case Study

Clinical features in adults with acquired cutis laxa: a retrospective review.

Published in:

British Journal of Dermatology, 2023, v. 188, n. 6, p. 800, doi. 10.1093/bjd/ljad043

By:

O'Connell, Katie A;
Schaefer, Morgan;
Atzmony, Lihi;
Vleugels, Ruth Ann;
Choate, Keith;
LaChance, Avery H;
Min, Michelle S

Publication type:

Article

Corrigenda.

Published in:: 2018
Publication type:: Correction Notice

Cutis laxa acquisita: novel insights into impaired elastic fibre regeneration.

Published in:

British Journal of Dermatology, 2017, v. 176, n. 3, p. 832, doi. 10.1111/bjd.15196

By:

Gkogkolou, P.;
Hildebrandt, K.;
Broekaert, S.;
Metze, D.;
Sengle, G.;
Böhm, M.

Publication type:

Article

A case of generalized acquired cutis laxa.

Published in:

2018

By:

Kim, Sung M.;
Lee, Suk Y.;
Kim, Jong B.;
Choi, Hoo M.;
Ro, Byung I.;
Cho, Han K.;
Ko, Eun J.

Publication type:

Case Study

A case of Marshall's syndrome and review of the literature.

Published in:

International Journal of Dermatology, 2015, v. 54, n. 6, p. e217, doi. 10.1111/ijd.12471

By:

Çalışkan, Ercan;
Açıkgöz, Gürol;
Yeniay, Yıldıray;
Özmen, İbrahim;
Gamsızkan, Mehmet;
Akar, Ahmet

Publication type:

Article

Generalized acquired cutis laxa with papular lesions.

Published in:

International Journal of Dermatology, 2015, v. 54, n. 2, p. e59, doi. 10.1111/ijd.12656

By:

Wang, Sheng

Publication type:

Article

Acral localized acquired cutis laxa.

Published in:

International Journal of Dermatology, 2013, v. 52, n. 8, p. 983, doi. 10.1111/j.1365-4632.2011.04955.x

By:

Martí, Nuria;
Monteagudo, Carlos;
Revert, Ángeles;
Reig, Irela;
Gámez, Lucía;
Jordá, Esperanza

Publication type:

Article

A rare case of secondary cutaneous lymphoplasmacytic lymphoma clinically presenting as acquired cutis laxa.

Published in:

Journal of Cutaneous Pathology, 2024, v. 51, n. 2, p. 135, doi. 10.1111/cup.14551

By:

Lim, Dong Jun;
Yang, Hee Joo;
Lee, Mi Young;
Lee, Woo Jin;
Won, Chong Hyun;
Chang, Sung Eun;
Lee, Mi Woo

Publication type:

Article

Rare clinical manifestations of leukemia cutis.

Published in:

2018

By:

Lamberti, Arianna;
Miracco, Clelia;
Scaramuzzino, Francesco;
Cinotti, Elisa;
Rubegni, Pietro;
Fimiani, Michele

Publication type:

Case Study

Frequency of cutis laxa-like clinical features and elastolysis in scleromyxedema: a retrospective clinicopathologic study of 19 patients with scleromyxedema.

Published in:

Journal of Cutaneous Pathology, 2016, v. 43, n. 3, p. 246, doi. 10.1111/cup.12657

By:

Gonzalez Santiago, Tania M.;
Lehman, Julia S.;
Buonaccorsi, J. Noelle;
Kalaaji, Amer N.;
Wieland, Carilyn N.

Publication type:

Article

A newborn with wrinkly skin: what is the diagnosis?

Published in:

Infant, 2021, v. 17, n. 3, p. 104

By:

Manjunatha, Chikkanayakanahalli M.;
Abourahma, Ahmed;
Ibhanesebhor, Samuel E.;
Mathews, Ashok Z.

Publication type:

Article

Genetics, Chronic Obstructive Pulmonary Disease, and the Arrow of Time.

Published in:

2019

By:

Calverley, Peter M. A.;
Walker, Paul P.

Publication type:

journal article

Cutis laxa (elastolysis) in a patient with Sjögren's syndrome.

Published in:

2015

By:

Işık, Metin;
Aydın, Çisel

Publication type:

Case Study

Primary anetoderma in an African child, a probably neglected disease in this population.

Published in:

Dermatologic Therapy, 2022, v. 35, n. 12, p. 1, doi. 10.1111/dth.15873

By:

Martos‐Cabrera, Luisa;
Hiltun, Ingrid;
Aróstegui‐Aguilar, Jorge;
Zarco‐Olivo, Carlos;
Torre, Covadonga;
Pinedo‐Moraleda, Fernando;
Galván‐Casas, Cristina

Publication type:

Article

Fractional photothermolysis treatment of digital cutis laxa reverses hand disability.

Published in:

Dermatologic Therapy, 2015, v. 28, n. 5, p. 279, doi. 10.1111/dth.12232

By:

Tian, Jack J.;
Hsiao, Wendy C.;
Worswick, Scott D.

Publication type:

Article

A Clinical Classification Scheme for Tracheobronchomegaly (Mounier-Kuhn Syndrome).

Published in:

Lung (0341-2040), 2015, v. 193, n. 5, p. 815, doi. 10.1007/s00408-015-9757-z

By:

Payandeh, Jennifer;
McGillivray, Barbara;
McCauley, Graeme;
Wilcox, Pearce;
Swiston, John;
Lehman, Anna

Publication type:

Article

Klinický fenotyp a genetická diagnostika raritného syndrómu cutis laxa u polystigmatizovaného novorodenca.

Published in:

Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie, 2022, v. 77, n. 4, p. 226, doi. 10.55095/cspediatrie2022/037

By:

Nina, Lenhartová;
Jana, Kršiaková;
Katarína, Maťašová;
Mirko, Zibolen

Publication type:

Article

In silico analysis of mutation spectrum of Ehlers–Danlos, osteogenesis imperfecta, and cutis laxa overlapping phenotypes in Iranian population.

Published in:

Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00479-5

By:

Khosravi, Teymoor;
Naghipoor, Karim;
Vaghefi, Fatemeh;
Falahati, Ali Mohammad;
Oladnabi, Morteza

Publication type:

Article

Acquired Cutis Laxa Type 2 (Marshall's Syndrome) Associated with Sweet's Syndrome: A Rare Entity.

Published in:

2024

By:

Samal, Abhipsa;
Bhoi, Aurobinda;
Mohanty, Jayashree;
Mishra, Chandraprava;
Basa, Adyasa;
Dash, Siddhartha

Publication type:

Letter to the Editor

Acquired localized cutis laxa: A case report and the role of plastic surgery.

Published in:: Indian Journal of Dermatology, 2019, v. 64, n. 1, p. 55, doi. 10.4103/ijd.IJD_14_18
Publication type:: Article

A 5-Year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited.

Published in:

Indian Journal of Dermatology, 2016, v. 61, n. 1, p. 81, doi. 10.4103/0019-5154.174031

By:

Dutta, Abhijit;
Ghosh, Sudip Kumar;
Ghosh, Arghyaprasun;
Roy, Sutirtha

Publication type:

Article

Cutis Laxa: A Report of Two Interesting Cases.

Published in:

Indian Journal of Dermatology, 2013, v. 58, n. 4, p. 324, doi. 10.4103/0019-5154.113986

By:

Subhabrata, Mitra;
Kumar, Agarwal Amit;
Kumar, Das Jayanta;
Asok, Gangopadhyay

Publication type:

Article

Supravalvular aortic stenosis with bicuspid aortic valve in a patient with cutis laxa syndrome.

Published in:

QJM: An International Journal of Medicine, 2023, v. 116, n. 5, p. 396, doi. 10.1093/qjmed/hcac283

By:

Velayutham, R;
Ahmed, A S;
Malathi, M;
Jinkala, S

Publication type:

Article

Identification of a novel intronic variant of ATP6V0A2 in a Han-Chinese family with cutis laxa.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09446-0

By:

Zhang, Ying;
Sun, Mei;
Li, Na;
Zhao, Yiran;
Zhang, Fang;
Shu, Jianbo;
Liu, Yang;
Cai, Chunquan

Publication type:

Article

Autosomal recessive cutis laxa type 1C with a homozygous LTBP4 splicing variant: a case report and update of literature.

Published in:

2022

By:

Mazaheri, Mahta;
Jahantigh, Hamid Reza;
Yavari, Mahdie;
Mirjalili, Seyed Reza;
Vahidnezhad, Hassan

Publication type:

Case Study

Coffin Siris Syndrome with Corpus Callosum Agenesia.

Published in:

Gazi Medical Journal, 2024, v. 35, p. 47

By:

Yüce, Vedat;
Demir, Şenol;
Hanoğlu, Onur;
Ceylan, Esra Hilal;
Geçkinli, Bilgen Bilge

Publication type:

Article

A Shared Pathogenesis? Elastic Tissue Degeneration in Two Generations: Co‐Occurrence of Acrokeratoelastoidosis and ARCL1A Cutis Laxa.

Published in:

2025

By:

Alrefaie, Sumayyah I;
Aljoudi, Sarah B.;
Nukaly, Houriah Y.;
Alhawsawi, Waseem K.;
Shadid, Asem;
AlNasser, Sultan;
Hariri, Jehad

Publication type:

Case Study

De Novo Autosomal Dominant Cutis Laxa Type 3 With Global Developmental Delay and Musculoskeletal Features of Refractory Rickets.

Published in:

2025

By:

Chandan, Subhangi;
Gohri, Jay;
Jolly, Arshia;
Chaurasia, Mayuri

Publication type:

Case Study

Autosomal recessive cutis laxa type Ib—Successful redo aortic root and arch replacement.

Published in:

2022

By:

Pees, Christiane;
Zimpfer, Daniel;
Radakovic, Sonja;
Beitzke, Dietrich;
Michel‐Behnke, Ina;
Laccone, Franco A.

Publication type:

Case Study

Acquired Cutis Laxa on the Upper Eyelids and Earlobes: A Case Report and Literature Review.

Published in:

Archives of Plastic Surgery, 2022, v. 49, n. 3, p. 418, doi. 10.1055/s-0042-1748657

By:

Kyoko Katsuren;
Ryogo Kuba;
Shogo Kasai;
Yusuke Shimizu

Publication type:

Article

Acquired cutis laxa type II (Marshall syndrome) in a 3‐month‐old boy.

Published in:

Pediatric Dermatology, 2022, v. 39, n. 2, p. 312, doi. 10.1111/pde.14734

By:

Sindhuja, Tekumalla;
Arunachalam, Narayanan;
Gupta, Vishal;
Agarwal, Shipra;
Gomathy, Sethuraman

Publication type:

Article