Acquired Cutis Laxa Type II (Marshall Syndrome) in an 18-Month-Old Child: A Case Report
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2009.01052.x/fullpdf
Reference11 articles.
1. Cutis laxa arising from frameshift mutations in exon of the elastin gene (ELN);Zhang;J Biol Chem,1999
2. A homozygosity for a missense mutation in fibulin-5 (FBLN5) results in severe form of cutis laxa;Loeys;Hum Molec Genet,2002
3. Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome;Hucthagowder;Am J Hum Genet,2006
4. Impaired glycosylation and cutis laxa caused by mutations in the vesicular H(+)-ATPase subunit ATP6V0A2;Kornnak;Nat Genet,2008
5. A novel frameshift mutation in Exon 23 of ATP7A (MNK) results in occipital syndrome and not in Menkes disease;Dagenais;Am J Hum Genet,2001
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1. Acquired cutis laxa secondary to acute generalized exanthematous pustulosis: A case report and mini‐review of literature;The Journal of Dermatology;2023-06-19
2. Acquired cutis laxa type II (Marshall syndrome) in a 3‐month‐old boy;Pediatric Dermatology;2021-12-20
3. Acquired cutis laxa secondary to sweet syndrome (marshall syndrome) in a 2-year-old child;Indian Journal of Paediatric Dermatology;2021
4. A case of Marshall's syndrome (postinflammatory elastolysis);Indian Journal of Dermatology, Venereology, and Leprology;2017
5. Acquired Disorders of Dermal Connective Tissue;Rook's Textbook of Dermatology, Ninth Edition;2016-10-09
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