Le Syndrome De Cutis Laxa : Clinique Et Pronostic A Propos DUn Cas
Keywords:
cutis laxa, genetic disease, malformation syndrome
Abstract
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References
B. Loeys, L. Van Maldergem, G. Mortier (2002) Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa. 11(18), 2113-8.
Morava E, Lefeber DJ, Urban Z (2008) Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation Eur J Hum Genet. 16(1), 28-35. https://doi.org/10.1038/sj.ejhg.5201947
Graul-Neumann LM, Hausser I, Essayie M, Rauch A, Kraus C (2008) Highly variable cutis laxa resulting from a dominant splicing mutation of the elastin gene. 146 A(8), 977-83.
Khakoo A, Thomas R, Trompeter R, Duffy P, Price R, Pope FM (1997) Congenital cutis laxa and lysyl oxidase deficiency Clin Genet. 51(2), 109-114.
V. Hill, C. Seymour, P. Mortimer (2000) Penicillamine-induced elastosis perforans serpiginosa and cutis laxa in Wilson's disease. 142(3), 560-561.
Gonzalez-Rodriguez AJ, Bella-Navarro R, Ramon D, Jorda-Cuevas E (2014) [Acquired cutis laxa associated with monoclonal gammopathy and lambda light chain deposition disease]. 20(5), 22611.
New HD, Callen JP (2011) Generalized acquired cutis laxa associated with multiple myeloma with biphenotypic IgG-? and IgA-? gammopathy following treatment of a nodal plasmacytoma Arch Dermatol. 147(3), 323.
O (2014) Acquired Cutis Laxa Associated With Heavy Chain Deposition Disease Involving Dermal Elastic Fibers.
Koklu E, Gunes T, Ozturk MA, Akcakus M, Buyukkayhan D, Kurtoglu S (2007) Cutis laxa associated with central hypothyroidism owing to isolated thyrotropin deficiency in a newborn Pediatr Dermatol. 24(5), 525-528.
Anderson CE, Finklestein JZ, Nussbaum E, Larson EJ, Halpern R, Uitto J (1984) Association of hemolytic anemia and early-onset pulmonary emphysema in three siblings J Pediatr. 105(2), 247-251.
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2016-05-24
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