Doctor insights on:
What Symptoms Of Peroneal Muscular Atrophy Are The Most Important
Weakness: Peroneal muscular atrophy is also know as charcot marie tooth disease (cmt), a genetic polyneuropathy that results in foot and leg weakness, potential for falls, secondary injury due to falls (e.g. Fractures), to name a few. Without getting into too much depth, much of the debility from this condition is due to the effects of foot/ankle/leg weakness. ...Read moreSee 1 more doctor answer
Atrophy usually refers to the skin-as you get older or if you have had alot of sun in the past-the dermis (that is the layer below the top layer which is called the epidermis) gets thinner and the skin looks more wrinked. Muscles and fat can also get thinner -this is another form of atrophy. Even the top layer gets thinner ...Read more
Several: Several including: muscle biopsy, peripheral nerve biopsy, electrodiagnostic studies, blood tests as well as imaging studies of the spine and possibly brain depending on other clinical symptoms or findings as well as the history of this problem and family history if pertinent. A neurologist would be the one to see for a complete evaluation. ...Read more
Weakness: Term implies a type of genetic disorder, which has several variations, and usually presents in early childhood. It may present as a "floppy infant", but can also cause a progressive generalized symmetrical weakness and muscular atrophy, more proximal than distal. Difficulty swallowing and breathing may be seen late in the disorder. ...Read more
Muscle vs motor neur: Duchenne muscular dystrophy is a disease of the muscles wherein the muscles degenerate and are replaced by fibrous and fatty tissue. Spinal muscular atrophy may look similar, but it is not an dystrophy. It is a disease of motor neurons. It is an inherited recessive disease. ...Read more
Muscles need nerves: Our muscles need the nerves that supply them or they get weak and "atropy." if the breathing muscles get so weak, then one can not breath and will have respiratory distress where the body can not move air or get rid of air. Hope this helps! take care! ...Read moreSee 1 more doctor answer
Heriditary Disease: A group of hereditary-genetic disease that result in muscular atrophy and weakness. They are progressive in nature. There are 4 types. Type i werdnig-hoffmann disease. Also type ii, iii , & the adult onset type iv. Treatment is supportive & physical therapy--to prevent contractures. ...Read more
Tough pathology...: Check out: http://www.Fightsma.Org/sma-guidebook/what-is-sma/ it is a genetic disease that causes degeneration and death of the motor neurons in the brain stem and spinal cord produces weakness in the muscles of swallowing, breathing, and limbs. There are different types with different severities. I hope this helps and check out that site, its a great site for general information about the disease. ...Read more
Spinal cord & muscle: Spinal muscular atrophy (sma) refers to a group of disorders that affect the nerve cells (anterior horn cells) that connect from the spinal cord to the muscles. There are several types depending on whether the disease starts in infancy, childhood, or young adulthood. Some genetic causes are known. There is no cure and treatment is supportive. For more info: www.Smafoundation.Org & www.Fsma.Org. ...Read more
Usually not: There are some experimental compounds that may prevent or delay atrophy in muscular dystrophy but nothing that uasually brings back muscles that have atrophied already. One should discuss preventative measures as well as possible treatmenst with a neuromuscular neurologist. ...Read more
Perhaps: Spinal muscular atrophy is a hereditary condition which may plateau and not rapidly progress as one gets older. Physical therapists could design exercise program, and perhaps acupuncture could assist in the control of aching and fatigue. But all in all, no true cure, and symptomatic approache best way so far. ...Read moreSee 1 more doctor answer
A neurodegeneration: Sbma is a serious problem in which a gene causes malfunction of male hormones and causes progressive damage to the nerves that control the muscles of the body. As time goes on, men with sbma may experience loss of fertility, impotence, severe weakness, trouble swallowing and breathing, numbness, all that worsen over time, typically in men and typically starting in adulthood. ...Read more
DOCTOR NAME: Because dr. William kennedy first described it in 1968. ...Read more
Kennedy's Diease: A debilitating neurodegenerative disease resulting in muscle cramps and progressive weakness due to degeneration of motor neurons in the brain stem and spinal cord. The condition is associated with mutation of the androgen receptor (ar) gene and is inherited as a x-linked recessive. As with many genetic disorders, no cure is known, although research continues. Described by dr kennedy in 1968. ...Read moreSee 2 more doctor answers
Muscle vs motor neur: Duchenne muscular dystrophy is a disease of the muscles wherein the muscles degenerate and are replaced by fibrous and fatty tissue. Spinal muscular atrophy may look similar, but it is not a dystrophy. It is a disease of motor neurons. It is an inherited recessive disease. ...Read more
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