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P.10.12 Difference of the mechanism of dysphagia between Duchenne muscular dystrophy and myotonic dystrophy type 1

✍ Scribed by Furuya, H.; Umemoto, G.; Kikuta, T.; Arahata, H.; Fujii, N.

Book ID
122358598
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
44 KB
Volume
23
Category
Article
ISSN
0960-8966

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Prenatal molecular diagnosis of inherite
Prenatal molecular diagnosis of inherited neuromuscular diseases: Duchenne/Becker muscular dystrophy, myotonic dystrophy type 1 and spinal muscular atrophy
✍ Esposito, Gabriella; Ruggiero, Raffaella; Savarese, Maria; Savarese, Giovanni; T πŸ“‚ Article πŸ“… 2013 πŸ› Walter de Gruyter GmbH & Co. KG 🌐 English βš– 314 KB

## Abstract **Background:** Neuromuscular disease is a broad term that encompasses many diseases that either directly, via an intrinsic muscle disorder, or indirectly, via a nerve disorder, impairs muscle function. Here we report the experience of our group in the counselling and molecular prenatal