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Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The maximum days the report can be obtained for the test Spinal Cerebral Ataxia (SCA) Type-10 is typically 14-21 days.

What are the prerequisites for the test Spinal Cerebral Ataxia (SCA) Type- 10

  • Genetic counseling
  • Fasting for at least 8 hours before the test
  • Medical history review
  • Physical examination
  • Family history review
  • Neurological examination

What are the measure values for the test Spinal Cerebral Ataxia (SCA) Type- 10

  • Gene: ATXN10
  • Chromosome: 22q13
  • Repeat Length: 11-22 CAG repeats
  • Normal Range: 11-22 CAG repeats
  • Pathogenic Range: >22 CAG repeats

What does this test Spinal Cerebral Ataxia (SCA) Type- 10 identify?

Spinal Cerebellar Ataxia (SCA) Type-10 Test

The Spinal Cerebellar Ataxia (SCA) Type-10 test is a diagnostic tool used to identify the presence of SCA Type-10 in an individual. SCA Type-10 is a rare genetic disorder that affects the nervous system, specifically the cerebellum, leading to symptoms such as poor coordination, balance problems, and difficulty with speech and swallowing.

The test typically involves genetic testing to detect mutations in the ATXN10 gene, which is associated with SCA Type-10. By identifying these mutations, healthcare providers can confirm a diagnosis of SCA Type-10 and develop a treatment plan to manage the symptoms and complications of the disorder.

Why is this test Spinal Cerebral Ataxia (SCA) Type- 10 taken?

Spinal Cerebral Ataxia (SCA) Type-10 Test

The test for Spinal Cerebral Ataxia (SCA) Type-10 is taken to diagnose and assess the severity of this specific type of ataxia. Ataxia is a neurological condition characterized by uncoordinated movement, and SCA Type-10 is a rare form of genetic ataxia.

Individuals may undergo this test if they exhibit symptoms such as unsteady gait, speech difficulties, tremors, and involuntary eye movements, which are common in SCA Type-10. A genetic test is typically used to confirm the presence of specific genetic mutations associated with this type of ataxia.

Early diagnosis of SCA Type-10 is crucial for appropriate management and treatment planning. This test can help healthcare providers determine the best course of action to improve quality of life and potentially slow the progression of the disease.

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