Rare Case of Ulnar-Mammary-Like Syndrome With Left Ventricular Tachycardia and Lack of TBX3 Mutation

“Heart–hand” type syndromes represent a group of rare congenital conditions that combine cardiac pathology (structural defect or arrhythmic disorder) and limb abnormality. Significant clinical variability and genetic heterogeneity typical for such syndromes complicate correct diagnosis, prognosis, a...

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Detalles Bibliográficos
Autores principales: Zlotina, Anna, Kiselev, Artem, Sergushichev, Alexey, Parmon, Elena, Kostareva, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013977/
https://www.ncbi.nlm.nih.gov/pubmed/29963074
http://dx.doi.org/10.3389/fgene.2018.00209

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013977/
https://www.ncbi.nlm.nih.gov/pubmed/29963074
http://dx.doi.org/10.3389/fgene.2018.00209

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