muscular dystrophy(redirected from facioscapulohu-meral muscular dystrophy)
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Related to facioscapulohu-meral muscular dystrophy: Limb girdle muscular dystrophy
n. Abbr. MD
Any of a group of progressive muscle disorders caused by a defect in one or more genes that control muscle function and characterized by gradual irreversible wasting of skeletal muscle.
(Pathology) a genetic disease characterized by progressive deterioration and wasting of muscle fibres, causing difficulty in walking
a hereditary disease characterized by gradual wasting of the muscles.
mus·cu·lar dys·tro·phy(mŭs′kyə-lər dĭs′trə-fē)
Any of several hereditary diseases in which a person's muscles gradually deteriorate, causing progressive weakness.
An inherited disorder in which there is a progressive wasting of muscle.
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|Noun||1.||muscular dystrophy - any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles|
congenital disease, genetic abnormality, genetic defect, genetic disease, genetic disorder, hereditary condition, hereditary disease, inherited disease, inherited disorder - a disease or disorder that is inherited genetically
Becker muscular dystrophy - a form of muscular dystrophy that sets in in adolescence or adulthood and progresses slowly but will affect all voluntary muscles; characterized by generalized weakness and muscle wasting that affects limb and trunk muscles first; similar to Duchenne's muscular dystrophy but less severe; inheritance is X-linked recessive (carried by females but affecting only males)
distal muscular dystrophy - a form of muscular dystrophy that sets in between 40 and 60 years of age and is characterized by weakness and wasting of the muscles of the hands and forearms and lower legs; inheritance is autosomal dominant
Duchenne's muscular dystrophy, pseudohypertrophic dystrophy - the most common form of muscular dystrophy; inheritance is X-linked recessive (carried by females but affecting only males)
limb-girdle muscular dystrophy - an autosomal recessive form of muscular dystrophy that appears anywhere from late childhood to middle age; characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle; usually progresses slowly with cardiopulmonary complications in the later stages
myotonia atrophica, myotonic dystrophy, myotonic muscular dystrophy, Steinert's disease - a severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant
oculopharyngeal muscular dystrophy - 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