Spinocerebellar ataxia type 2 (SCA2

Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement.

People with this condition initially experience problems with coordination and balance (ataxia).
Other early signs and symptoms of SCA2 include speech and swallowing difficulties, rigidity, tremors, and weakness in the muscles that control eye movement (ophthalmoplegia).

Eye muscle weakness leads to a decreased ability to make rapid eye movements (saccadic slowing).
Over time, individuals with SCA2 may develop loss of sensation and weakness in the limbs (peripheral neuropathy), muscle wasting (atrophy), uncontrolled muscle tensing (dystonia), and involuntary jerking movements (chorea).

Individuals with SCA2 may have problems with short term memory, planning, and problem solving, or experience an overall decline in intellectual function (dementia).

Signs and symptoms of the disorder typically begin in mid-adulthood but can appear anytime from childhood to late adulthood. People with SCA2 usually survive 10 to 20 years after symptoms first appear.

ผลลัพธ์ (อังกฤษ) 2:

Spinocerebellar ataxia Type 2 (SCA2) is a condition characterized by progressive Problems with Movement. People with this condition initially Experience Problems with coordination and balance (ataxia). Other Early Signs and symptoms of SCA2 include Speech and swallowing difficulties, rigidity, tremors, and. weakness in the Muscles that Control Eye Movement (ophthalmoplegia). Eye Muscle weakness Leads to a Decreased ability to Make Rapid Eye Movements (saccadic slowing). Over time, individuals with SCA2 May develop Loss of Sensation and weakness in the limbs (Peripheral neuropathy). , Muscle wasting (atrophy), uncontrolled Muscle tensing (dystonia), and involuntary jerking Movements (Chorea). Individuals with SCA2 May have Problems with short term memory, planning, and Problem Solving, or Experience an overall decline in Intellectual function (dementia). . Signs and symptoms of the Disorder typically BEGIN in Mid-from childhood to adulthood but Can appear Anytime Late adulthood. People with SCA2 usually survive 10 to 20 years after symptoms first appear.

ผลลัพธ์ (อังกฤษ) 3:

Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement.

People with. This condition initially experience problems with coordination and balance (ataxia).
Other early signs and symptoms of. SCA2 include speech and swallowing difficulties rigidity tremors,,, weakness and in the muscles that control eye movement. (ophthalmoplegia).

.Eye muscle weakness leads to a decreased ability to make rapid eye movements (saccadic slowing).
Over time individuals,, With SCA2 may develop loss of sensation and weakness in the limbs (peripheral neuropathy), muscle wasting (atrophy), uncontrolled. Muscle tensing (dystonia), and involuntary jerking movements (chorea).

Individuals with SCA2 may have problems with short. Term memory planning,,And problem solving or experience, an overall decline in intellectual function (dementia).

Signs and symptoms of the disorder. Typically begin in mid-adulthood but can appear anytime from childhood to late adulthood. People with SCA2 usually survive 10 to 20 years. After symptoms first appear.