
______ is not a form of muscular dystrophy
A. Lunar dystrophy
B. Myotonic dystrophy
C. Duchenne muscular dystrophy
D. Facioscapulohumeral dystrophy
Answer
343.5k+ views
Hint:
Muscle loss and weakening progress over time in myotonic dystrophy. A common symptom of this illness is myotonia, which is the inability to relax a particular muscle after use. For instance, a person can find it challenging to let go of a handle or doorknob. An umbrella term for nine hereditary illnesses that gradually weaken and degenerate the muscles utilized for voluntary movement is muscular dystrophy (MD). One of the muscular dystrophies is myotonic dystrophy (DM). It is the most typical form observed in adults and is likely one of the typical forms in general.
Even at a young age, respiratory and cardiac problems can be fatal in the most severe situations. In general, the more severe the symptoms are likely to be, the younger the person is when they first manifest.
Complete answer:
Patients with Duchenne muscular dystrophy have a poor prognosis. By the time they are teenagers, the majority are using wheelchairs, and they rarely live past their thirties. The illness has no known treatment. Congenital muscular dystrophy, a rare kind of muscular dystrophy with numerous subtypes, includes Fukuyama-type congenital muscular dystrophy (FCMD). It is an autosomal recessive characteristic that is inherited. This disorder's signs show up at birth and develop gradually. DMD is generally not unpleasant, but occasionally cramps can be brought on by muscle issues.
So, lunar dystrophy is not a form of muscular dystrophy.
Option ‘A’ is correct
Note:
A condition known as facioscapulohumeral muscular dystrophy causes wasting and muscle weakening (atrophy). The muscles in the face, shoulders, and upper arms that are most frequently affected give rise to this condition's name (humeral). Facioscapulohumeral muscular dystrophy is still fatal at this time. Treatments are used to reduce symptom severity and enhance the quality of life.
Weakness of the face muscles, the scapular stabilizers, or the foot's dorsiflexion is the usual symptom of facioscapulohumeral muscular dystrophy (FSHD). The severity can vary greatly.
Muscle loss and weakening progress over time in myotonic dystrophy. A common symptom of this illness is myotonia, which is the inability to relax a particular muscle after use. For instance, a person can find it challenging to let go of a handle or doorknob. An umbrella term for nine hereditary illnesses that gradually weaken and degenerate the muscles utilized for voluntary movement is muscular dystrophy (MD). One of the muscular dystrophies is myotonic dystrophy (DM). It is the most typical form observed in adults and is likely one of the typical forms in general.
Even at a young age, respiratory and cardiac problems can be fatal in the most severe situations. In general, the more severe the symptoms are likely to be, the younger the person is when they first manifest.
Complete answer:
Patients with Duchenne muscular dystrophy have a poor prognosis. By the time they are teenagers, the majority are using wheelchairs, and they rarely live past their thirties. The illness has no known treatment. Congenital muscular dystrophy, a rare kind of muscular dystrophy with numerous subtypes, includes Fukuyama-type congenital muscular dystrophy (FCMD). It is an autosomal recessive characteristic that is inherited. This disorder's signs show up at birth and develop gradually. DMD is generally not unpleasant, but occasionally cramps can be brought on by muscle issues.
So, lunar dystrophy is not a form of muscular dystrophy.
Option ‘A’ is correct
Note:
A condition known as facioscapulohumeral muscular dystrophy causes wasting and muscle weakening (atrophy). The muscles in the face, shoulders, and upper arms that are most frequently affected give rise to this condition's name (humeral). Facioscapulohumeral muscular dystrophy is still fatal at this time. Treatments are used to reduce symptom severity and enhance the quality of life.
Weakness of the face muscles, the scapular stabilizers, or the foot's dorsiflexion is the usual symptom of facioscapulohumeral muscular dystrophy (FSHD). The severity can vary greatly.
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