Aplasie cutanée congénitale, défaut de compaction du ventricule gauche et troubles du rythme cardiaque graves : un nouveau cas de syndrome MLS (microphtalmia with linear skin defects)-Reference-Cited by-同舟云学术

Aplasie cutanée congénitale, défaut de compaction du ventricule gauche et troubles du rythme cardiaque graves : un nouveau cas de syndrome MLS (microphtalmia with linear skin defects)

Published:2003-03 Issue:3 Volume:10 Page:224-226
ISSN:0929-693X
Container-title:Archives de Pédiatrie
language:fr
Short-container-title:Archives de Pédiatrie

Author:

Kherbaoui-Redouani L,Eschard C,Bednare N,Morville P

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference11 articles.

1. Two 46,XX,t(X;Y) females with linear skin defects and congenital microphtalmia: a new syndrome at Xp22-3;al-Gazali;J Med Genet,1990

2. MIDAS syndrome (microphtalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome;Happle;Am J Med Genet,1993

3. Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22;Zvulunov;Br J Dermatol,1998

4. Female infant with oncocytic cardiomyopathy and microphtalmia with linear skin defects (MLS): a clue to the pathogenesis of oncocytic cardiomyopathy?;Bird;Am J Med Genet,1994

5. Linear skin defects associated with microphtalmia and other malformations, with chromosome deletion Xp22-1;Eng;J Am Acad Dermatol,1994

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Implantable Cardioverter Defibrillators in Infants and Toddlers: Indications, Placement, Programming, and Outcomes;Circulation: Arrhythmia and Electrophysiology;2022-02

2. Left Ventricular Noncompaction;Clinical Cardiogenetics;2020

3. Inherited Cardiac Muscle Disorders: Left Ventricular Noncompaction;Cardiovascular Genetics and Genomics;2018

4. Left ventricular noncompaction cardiomyopathy: cardiac, neuromuscular, and genetic factors;Nature Reviews Cardiology;2017-01-12

5. Left Ventricular Noncompaction;Clinical Cardiogenetics;2016