Progressive Retina Atrophy is a dominant genetic disorder.
sezures
Lou Gehrigs disease
Spinal muscular atrophy is an autosomal recessive disease. The severity of spinal muscular atrophy varies, and is the most common genetic cause of infant death.
Sven Brandt has written: 'Werdnig-Hoffmann's infantile progressive muscular atrophy' -- subject(s): Atrophy, Muscular, Diseases, In infancy and childhood, Infants, Muscular atrophy
Often, a disorder of the motor neurons results in progressive muscle atrophy (shrinking and wasting) of some, if not all, the muscles of the body. Muscle twitching (fasciculation) is common among these disorders
Severe cortical atrophy is also known as dementia. The symptoms of dementia are a progressive impairment of memory and intellectual function that is severe enough to interfere with the activities of daily living.
Atrophy is progressive weakening and size reduction of muscle tissue which is usually the result of disease or disuse.
No. Huntington's Disease is a pathological process affecting subcortical structures, not the cerebellar cortex. It does cause generalized atrophy of the cerebral cortex, over time, however. It is a genetic disorder, autosomal dominant in its transmission process, and occurring on chromosome number 4.
SMA = Spinal muscular atrophy. There are different types of SMA, all I believe are genetic and are autosomal recessive. They cause weakness and paralysis in the lower motor neurons.
The cause of MSA has not been identified. MSA occurs in the general population in a sporadic manner. The disorder is degenerative and progressively worsens.
She has a muscular atrophy.
Atrophy is the wearing away of an organ or tissue because of lack of use. Bone Atrophy, obviously, is atrophy of bones.