Oculopharyngeal Muscular Dystrophy
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Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Oculopharyngeal dystrophy (OPD, or oculopharyngeal muscular dystrophy) is an autosomal dominant disorder which appears in early middle age (sixth decade) in individuals with a mutation on the PABPN1 gene. It has also known as obligatory post meal dip. Progressive ptosis (drooping of eyelids)and weakness of the extraocular muscles is the initial clinical finding which continues until paralysis of all eye movements occurs; however, pupillary reactions remain unaffected.…mehr

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Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Oculopharyngeal dystrophy (OPD, or oculopharyngeal muscular dystrophy) is an autosomal dominant disorder which appears in early middle age (sixth decade) in individuals with a mutation on the PABPN1 gene. It has also known as obligatory post meal dip. Progressive ptosis (drooping of eyelids)and weakness of the extraocular muscles is the initial clinical finding which continues until paralysis of all eye movements occurs; however, pupillary reactions remain unaffected. Dysphagia (difficulty swallowing), facial weakness and proximal limb weakness develops later on in the disease.