Myotonic dystrophy-2: Unusual phenotype due to a small CCTG-expansion

Myotonic dystrophy-2: Unusual phenotype due to a small CCTG-expansion

Myotonic dystrophy type 2 (MD2) is a multisystem disease, predominantly affecting the proximal limb muscles, eyes, endocrine organs, heart and intestines. Longterm asymptomatic creatine kinase (hyper-CKemia) of more than 20 years duration, in association with hyperlipidemia and diabetes, as a manife...

Full description

Bibliographic Details
Main Authors: Finsterer J, Stöllberger C, Reining-Festa A, Loewe-Grgurin M, Gencik M
Format: Article
Language:English
Published: Sciendo 2018-12-01
Series:Balkan Journal of Medical Genetics
Subjects:
cardiac involvement
creatine kinase (hyper-ckemia)
multisystem disease
myotonia
neuromuscular
znf9 gene
Online Access:https://doi.org/10.2478/bjmg-2018-0024

Internet

https://doi.org/10.2478/bjmg-2018-0024

Similar Items