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

Samia El Haouzi; Karman Abdellouahed; Rajae Daoudi

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

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Karman Abdellouahed

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Rajae Daoudi

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

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References

10 Cites in Article

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1. 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. Hum Mol Genet, 11(9), 2113-2118.
2. E Morava,D Lefeber,Z Urban (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.
3. 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. Am J Med Genet A, 146(8), 977-983.
4. A Khakoo,R Thomas,R Trompeter,P Duffy,R Price,F Pope (1997). Congenital cutis laxa and lysyl oxidase deficiency. Clin Genet, 51(2), 109-114.
5. V Hill,C Seymour,P Mortimer (2000). Penicillamine-induced elastosis perforans serpiginosa and cutis laxa in Wilson’s disease. British Journal of Dermatology, 142(3), 560-561.
6. 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. Dermatology Online Journal, 20(5), 22611.
7. 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. Archives of Dermatology, 147(3), 323.
8. John O’malley,Vivette D’agati,William Sherman,Marc Grossman (2014). Acquired Cutis Laxa Associated With Heavy Chain Deposition Disease Involving Dermal Elastic Fibers. JAMA Dermatology, 150(11), 1192.
9. 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. Pediatr Dermatol, 525-528.
10. 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. The Journal of Pediatrics, 105(2), 247-251.

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Funding

No external funding was declared for this work.

Conflict of Interest

The authors declare no conflict of interest.

Ethical Approval

No ethics committee approval was required for this article type.

Data Availability

Not applicable for this article.

How to Cite This Article

Samia El Haouzi, Karman Abdellouahed, Rajae Daoudi. 2016. "Le Syndrome De Cutis Laxa : Clinique Et Pronostic A Propos DUn Cas". Global Journal of Medical Research - K: Interdisciplinary GJMR-K Volume 16 (GJMR Volume 16 Issue K4).

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Journal Specifications

Crossref Journal DOI 10.17406/gjmra

Print ISSN 0975-5888

e-ISSN 2249-4618

Keywords

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Classification

GJMR-K Classification NLMC Code: QV 60

QV 75

Submission ReceivedDecember 12, 2015
Peer Review Double Blind
Handling Editor
Accepted January 1, 2016
Published January 15, 2016

Version of record

v1.2

Issue date

July 22, 2016

Language

French

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Article Matrices

Total Score: 133

Country: France

Subject: Global Journal of Medical Research - K: Interdisciplinary

Authors: Samia El Haouzi, Karman Abdellouahed, Rajae Daoudi (PhD/Dr. count: 0)

View Count (all-time): 352

Total Views (Real + Logic): 1331

Total Downloads (simulated): 96

Publish Date: 2016 01, Fri

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Total Views: 1.3K

Total Downloads: 96

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