Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0013362 (
dysarthria
)
3,768
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Facioscapulohumeral muscular dystrophy
(
FSHD
) is a common inherited muscular dystrophy presented clinically with slowly progressive weakness and wasting of facial and limb muscles and rare bulbar muscle involvement. We present herein a 70-year-old man who was a known case of
FSHD
with complaint of 15-day history of progressive difficulty in chewing and
dysarthria
and was found to have myasthenia gravis. Related literatures have been also reviewed.
...
PMID:A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis. 2425 Aug 56
