Definition of Oculopharyngeal. Meaning of Oculopharyngeal. Synonyms of Oculopharyngeal

Here you will find one or more explanations in English for the word Oculopharyngeal. Also in the bottom left of the page several parts of wikipedia pages related to the word Oculopharyngeal and, of course, Oculopharyngeal synonyms and on the right images related to the word Oculopharyngeal.

Definition of Oculopharyngeal

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Meaning of Oculopharyngeal from wikipedia

- Oculopharyngeal muscular dystrophy (OPMD) is a rare form of muscular dystrophy with symptoms generally starting when an individual is 40 to 50 years old...
- weakness in muscles or nerve damage, such as myasthenia gravis or oculopharyngeal muscular dystrophy. Exposure to the toxins in some snake venoms, such...
- PMC 2573281. PMID 18799579. "Oculopharyngeal muscular dystrophy". Genetics Home Reference. National Library of Medicine. "Oculopharyngeal Muscular Dystrophy"....
- Facioscapulohumeral dystrophy (FSHD) Congenital dystrophy (CMD) Distal (DD) Oculopharyngeal dystrophy (OPMD) Emery-Dreifuss (EDMD) Major systems of the human body...
- end of the coding region of this gene leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD) disease. Multiple splice variants have been...
- Oculomelic amyoplasia Oculomotor nerve palsy Oculopalatoskeletal syndrome Oculopharyngeal muscular dystrophy Oculorenocerebellar syndrome Odonto onycho dysplasia...
- Hepatitis B (under development with partner Biomics Biotechnologies)) Oculopharyngeal muscular dystrophy (OPMD) "Benitec Biopharma". Australian Securities...
- skeletal muscles, including the heart, endocrine organs, and eyes. Oculopharyngeal muscular dystrophy 164300 PABPN1 AD, rarely AR 40–50 years Eye muscles...
- 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)...
- leukodystrophy Endocrinology, neurology Autosomal recessive ARSA 1/50 Yemen  Oculopharyngeal muscular dystrophy Neurology Autosomal, recessive or dominant PABPN1...