Le Syndrome De Cutis Laxa : Clinique Et Pronostic A Propos DUn Cas

Samia  El Haouzi; Karman Abdellouahed; Rajae Daoudi

Authors

Samia El Haouzi
Karman Abdellouahed
Rajae Daoudi

Keywords:

cutis laxa, genetic disease, malformation syndrome

Abstract

Abstract not found

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How to Cite

Le Syndrome De Cutis Laxa : Clinique Et Pronostic A Propos DUn Cas. (2016). Global Journal of Medical Research, 16(K4), 21-24. https://medicalresearchjournal.org/index.php/GJMR/article/view/100719

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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(9), 2113-2118.

E Morava, D Lefeber, Z Urban (2008) Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation. 16(1), 28-35.

L Graul-Neumann, I Hausser, M Essayie, A Rauch, C Kraus (2008) Highly variable cutis laxa resulting from a dominant splicing mutation of the elastin gene. 146(8), 977-983.

A Khakoo, R Thomas, R Trompeter, P Duffy, R Price, F Pope (1997) Congenital cutis laxa and lysyl oxidase deficiency. 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.

Antonio Gonzalez-Rodriguez, Rebeca Bella-Navarro, Dolores Ramon Quiles, Esperanza Jorda-Cuevas (2014) Cutis laxa adquirido asociado a gammapatía monoclonal y enfermedad por depósito de cadenas ligeras lambda. 20(5), 22611.

H New, Jeffrey Callen (2011) Generalized Acquired Cutis Laxa Associated With Multiple Myeloma With Biphenotypic IgG- λ and IgA-κ Gammopathy Following Treatment of a Nodal Plasmacytoma. 147(3), 323.

John O'malley, Vivette D'agati, William Sherman, Marc Grossman (2014) Acquired Cutis Laxa Associated With Heavy Chain Deposition Disease Involving Dermal Elastic Fibers. 150(11), 1192.

E Koklu, T Gunes, M Ozturk, M Akcakus, D Buyukkayhan, S Kurtoglu (2007) Cutis laxa associated with central hypothyroidism owing to isolated thyrotropin deficiency in a newborn. (5), 525-528.

Carol Anderson, Jerry Finklestein, Eliezer Nussbaum, Eunice Larson, Roy Halpern, Jouni Uitto, Kouichi Tanaka (1984) Association of hemolytic anemia and early-onset pulmonary emphysema in three siblings. 105(2), 247-251.