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Oculopharyngeal Muscular Dystrophy

Oculopharyngeal Muscular Dystrophy: Introduction

Oculopharyngeal Muscular Dystrophy: A group of genetic muscle-wasting diseases which affects mainly the eyes and throat. Weakness in limb and facial muscles can occur in later stages. More detailed information about the symptoms, causes, and treatments of Oculopharyngeal Muscular Dystrophy is available below.

Symptoms of Oculopharyngeal Muscular Dystrophy

  • Progressive ptosis
  • Progressive swallowing difficulty
  • Characteristic face
  • Progressive weakness of eye muscles
  • Progressive weakness of throat muscles
  • more symptoms...»

See full list of 13 symptoms of Oculopharyngeal Muscular Dystrophy

Oculopharyngeal Muscular Dystrophy: Complications

Review possible medical complications related to Oculopharyngeal Muscular Dystrophy:

Disease Topics Related To Oculopharyngeal Muscular Dystrophy

Research the causes of these diseases that are similar to, or related to, Oculopharyngeal Muscular Dystrophy:

Medical Textbooks Online about Oculopharyngeal Muscular Dystrophy

Medical Books Excerpts
  • DYSPHAGIA
  • "Algorithmic Diagnosis of Symptoms and Signs" (2003)
  • PTOSIS
  • "Algorithmic Diagnosis of Symptoms and Signs" (2003)
  • Ptosis
  • "In a Page: Signs and Symptoms" (2004)
  • Dysphagia
  • "In A Page: Pediatric Signs and Symptoms" (2007)
  • Ptosis
  • "In A Page: Pediatric Signs and Symptoms" (2007)
  • PTOSIS
  • "Differential Diagnosis in Primary Care" (2007)
  • Dysphagia
  • "Handbook of Signs & Symptoms (Third Edition)" (2006)
  • Ptosis
  • "Handbook of Signs & Symptoms (Third Edition)" (2006)
  • Ptosis
  • "Professional Guide to Diseases (Eighth Edition)" (2005)
  • Dysphagia
  • "Professional Guide to Signs & Symptoms (Fifth Edition)" (2006)
  • Ptosis
  • "Professional Guide to Signs & Symptoms (Fifth Edition)" (2006)
  • Dysphagia
  • "The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter" (2000)
  • Ptosis
  • "Field Guide to Bedside Diagnosis" (2007)
  • Dysphagia
  • "Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series" (2007)
  • Dysphagia
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses" (2007)
  • Ptosis
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses" (2007)
  • Ptosis
  • "The Diagnostic Approach to Symptoms and Signs in Pediatrics" (2006)
  • Dysphagia
  • "Nursing: Interpreting Signs and Symptoms" (2007)
  • Ptosis
  • "Nursing: Interpreting Signs and Symptoms" (2007)
  • PTOSIS
  • "Differential Diagnosis in Primary Care" (2007)
 

Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Less Common Symptoms of Oculopharyngeal Muscular Dystrophy

Read more about symptoms of Oculopharyngeal Muscular Dystrophy

Wrongly Diagnosed with Oculopharyngeal Muscular Dystrophy?

Oculopharyngeal Muscular Dystrophy: Research Doctors & Specialists

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Causes of Oculopharyngeal Muscular Dystrophy

Read more about causes of Oculopharyngeal Muscular Dystrophy

More information about causes of Oculopharyngeal Muscular Dystrophy:

Evidence Based Medicine Research for Oculopharyngeal Muscular Dystrophy

Medical research articles related to Oculopharyngeal Muscular Dystrophy include:

Click here to find more evidence-based articles on the TRIP Database

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Prognosis for Oculopharyngeal Muscular Dystrophy

Prognosis for Oculopharyngeal Muscular Dystrophy: The condition usually progresses slowly.

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Reseach about Oculopharyngeal Muscular Dystrophy

Visit our research pages for current research about Oculopharyngeal Muscular Dystrophy treatments.

Oculopharyngeal Muscular Dystrophy: Broader Related Topics

Types of Oculopharyngeal Muscular Dystrophy

Stories from Users Related to Oculopharyngeal Muscular Dystrophy

User Interactive Forums

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Definitions of Oculopharyngeal Muscular Dystrophy:

An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy. - (Source - Diseases Database)

A form of muscular dystrophy that usually begins between early adulthood and middle age and first affects muscles of the eyelid and throat; progresses slowly with swallowing problems common as the disease progresses; inheritance is autosomal dominant - (Source - WordNet 2.1)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Oculopharyngeal Muscular Dystrophy as a "rare disease".
Source - Orphanet

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