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

2021 ◽  
Author(s):  
Tekumalla Sindhuja ◽  
Narayanan Arunachalam ◽  
Vishal Gupta ◽  
Shipra Agarwal ◽  
Sethuraman Gomathy
Keyword(s):  
Cutis Laxa ◽  
Type Ii

Acquired Cutis Laxa Type II (Marshall Syndrome) in an 18-Month-Old Child: A Case Report

2010 ◽  
Vol 27 (1) ◽  
pp. 89-91 ◽  
Author(s):  
Mansoor Haider ◽  
Abdullah Alfadley ◽  
Razan Kadry ◽  
Abdulmonem Almutawa
Keyword(s):  
Case Report ◽  
Cutis Laxa ◽  
Type Ii

Cutis laxa complicating Ehlers-Danlos syndrome type II

1996 ◽  
Vol 21 (2) ◽  
pp. 135-137 ◽  
Author(s):  
L.S. OSTLERE ◽  
F.M. POPE ◽  
C.A. HOLDEN
Keyword(s):  
Cutis Laxa ◽  
Syndrome Type ◽  
Type Ii ◽  
Ehlers Danlos Syndrome ◽  
Danlos Syndrome

Male with type II autosomal recessive cutis laxa

2008 ◽  
Vol 45 (1) ◽  
pp. 40-43 ◽  
Author(s):  
Kiyoshi Imaizumi ◽  
Kenji Kurosawa ◽  
Yoshio Makita ◽  
Mitsuo Masuno ◽  
Yoshikazu Kuroki
Keyword(s):  
Autosomal Recessive ◽  
Cutis Laxa ◽  
Type Ii

Type II autosomal recessive cutis laxa: Report of another patient and molecular studies concerning three candidate genes

2008 ◽  
Vol 146A (21) ◽  
pp. 2740-2745 ◽  
Author(s):  
Daniel Zanetti Scherrer ◽  
Fabiana Alexandrino ◽  
Maria Letícia Cintra ◽  
Edi Lúcia Sartorato ◽  
Carlos Eduardo Steiner
Keyword(s):  
Candidate Genes ◽  
Autosomal Recessive ◽  
Cutis Laxa ◽  
Type Ii ◽  
Molecular Studies

scholarly journals Type II acquired cutis laxa associated with recurrent urticarial vasculitis: brief report

2020 ◽  
Vol 16 (1) ◽  
Author(s):  
Amelia Nabatanzi ◽  
Siqi Da ◽  
Musa Male ◽  
Siyuan Chen ◽  
Changzheng Huang
Keyword(s):  
Family History ◽  
Inflammatory Cells ◽  
Cutis Laxa ◽  
Elastic Fibers ◽  
Type Ii ◽  
Urticarial Vasculitis ◽  
Case Presentation ◽  
History Of ◽  
Skin Wrinkling ◽  
Chemical Mediators

Abstract Background Cutis laxa is a connective tissue disease characterized by loose, wrinkled, and redundant skin. It is either inherited or acquired. In most cases, acquired cutis laxa is associated with neoplasms, drugs, and autoimmune diseases. We present a rare case of acquired cutis laxa following a recurrent urticaria-like eruption in the absence of an autoimmune disease, neoplasm, drugs and or syndrome. Case presentation We report a case of a 45-year-old Chinese lady with a 1-year history of widespread pruritic urticarial eruption and a 6-month history of progressive skin wrinkling. On examination, the patient appeared older than her actual age, with apparent wrinkling on the mid-torso with generalized smooth, erythematous macules and wheals. A family history of similar conditions was absent. Biopsy revealed hypersensitivity and atrophy. Following the Food and Drug Administration (FDA) guidelines, we administered antihistamines, which relieved the itching, but her hyperpigmentation and cutis laxa never improved. Conclusion Our case shows that the decrease of elastic fibers may be associated with the infiltration of inflammatory cells in the dermis. This supports the hypothesis that chemical mediators may play a major role in the destruction of elastic fibers, thus causing cutis laxa. In addition, we advise practitioners to take a complete clinical and family history to determine if the condition is inherited or acquired.

Cutis Laxa Type II with Mutation in the Pyrroline-5-Carboxylate Reductase 1 Gene

2013 ◽  
Vol 30 (6) ◽  
pp. e265-e267 ◽  
Author(s):  
Nayereh Nouri ◽  
Omid Aryani ◽  
Narges Nouri ◽  
Behnam Kamalidehghan ◽  
Massoud Houshmand
Keyword(s):  
Cutis Laxa ◽  
Type Ii ◽  
Carboxylate Reductase

scholarly journals Cutis laxa autosomal recessive type II or wrinkly skin syndrome?

2016 ◽  
Vol 7 (5) ◽  
pp. 440
Author(s):  
Pooja Arora ◽  
Payal Chakravarty ◽  
Deepshikha Khanna ◽  
Ruchika Gupta
Keyword(s):  
Autosomal Recessive ◽  
Cutis Laxa ◽  
Type Ii ◽  
Recessive Type

scholarly journals Autosomal recessive cutis laxa Type II: Report of novel mutation in a child

2017 ◽  
Vol 8 (5) ◽  
pp. 352
Author(s):  
Rakesh Kumar ◽  
Sheetal Sharda ◽  
Vimlesh Soni ◽  
Kaniyappan Nambiyar
Keyword(s):  
Autosomal Recessive ◽  
Novel Mutation ◽  
Cutis Laxa ◽  
Type Ii
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