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Oculopharyngeal muscular dystrophy (OPMD) is a rare form of
muscular dystrophy with
symptoms generally starting when an
individual is 40 to 50
years old...
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weakness in
muscles or
nerve damage, such as
myasthenia gravis or
oculopharyngeal muscular dystrophy.
Exposure to the
toxins in some
snake venoms, such...
-
classified as an
orphan disease,
there is
currently no
therapy for
oculopharyngeal muscular dystrophy (OPMD), as it is
caused by a
mutation in the poly(A)...
- end of the
coding region of this gene
leads to
autosomal dominant oculopharyngeal muscular dystrophy (OPMD) disease.
Multiple splice variants have been...
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Facioscapulohumeral dystrophy (FSHD)
Congenital dystrophy (CMD)
Distal (DD)
Oculopharyngeal dystrophy (OPMD) Emery-Dreifuss (EDMD)
Major systems of the
human body...
- PMC 2573281. PMID 18799579. "
Oculopharyngeal muscular dystrophy".
Genetics Home Reference.
National Library of Medicine. "
Oculopharyngeal Muscular Dystrophy"....
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skeletal muscles,
including the heart,
endocrine organs, and eyes.
Oculopharyngeal muscular dystrophy 164300 PABPN1 AD,
rarely AR 40–50
years Eye muscles...
-
Hepatitis B (under
development with
partner Biomics Biotechnologies))
Oculopharyngeal muscular dystrophy (OPMD) "Benitec Biopharma".
Australian Securities...
-
leukodystrophy Endocrinology,
neurology Autosomal recessive ARSA 1/50
Yemen Oculopharyngeal muscular dystrophy Neurology Autosomal,
recessive or
dominant PABPN1...
- Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic,
oculopharyngeal, distal, and Emery–Dreifuss
muscular dystrophies. The act established...
