Oculopharyngeal muscular dystrophy
volume
folder open
wordList
Close
British pronunciation/ˈɒkjʊlˌɒfɑːɹˌɪndʒiəl mˈʌskjʊlə dˈɪstɹəfi/
American pronunciation/ˈɑːkjʊlˌɑːfɑːɹˌɪndʒiəl mˈʌskjʊlɚ dˈɪstɹəfi/

Definition & Bedeutung von "oculopharyngeal muscular dystrophy"

Oculopharyngeal muscular dystrophy
01

okulopharyngeale Muskeldystrophie

a rare genetic disorder that primarily affects the muscles of the eyes and throat
folder open
wordList
Close

What is "oculopharyngeal muscular dystrophy"?

Oculopharyngeal muscular dystrophy (OPMD) is a genetic disorder that affects the muscles of the eyes and throat. It is characterized by progressive weakness and wasting of these muscles, leading to difficulties with swallowing, speaking, and controlling eye movements. OPMD typically starts in adulthood, usually between the ages of 40 and 60, and can vary widely in intensity between individuals. It is caused by changes in genes that are involved in muscle function. Treatment for OPMD focuses on managing symptoms and improving quality of life. This may include speech therapy to improve swallowing and communication, dietary changes to make swallowing easier, and assistive devices such as special utensils or feeding tubes if swallowing becomes very difficult. While there is currently no cure for OPMD, ongoing research may lead to new treatments in the future.

download-mobile-app
Laden Sie unsere mobile App herunter
Langeek Mobile Application
download application
Teilbare Karten

Definition & Bedeutung von "Oculopharyngeal muscular dystrophy"
Copyright © 2024 Langeek Inc. | All Rights Reserved |Privacy Policy
Copyright © 2024 Langeek Inc.
All Rights Reserved
instagramtelegramlinkedintwitterfacebook
langeek application

Download Mobile App

stars

app store