hereditary cerebellar ataxia Synonyms

No Synonyms and anytonyms found

hereditary cerebellar ataxia Meaning

Wordnet

hereditary cerebellar ataxia (n)

nervous disorder of late childhood and early adulthood; characterized by ataxic gait and hesitating or explosive speech and nystagmus

hereditary cerebellar ataxia Sentence Examples

  1. Hereditary cerebellar ataxia (HCA) is a genetic disorder characterized by progressive degeneration of the cerebellum.
  2. HCA can affect individuals at any age, with the onset of symptoms typically occurring in the third or fourth decade of life.
  3. The most common symptoms of HCA include difficulty with balance and coordination, slurred speech, and involuntary eye movements.
  4. HCA is caused by mutations in genes that encode proteins essential for proper cerebellar function.
  5. HCA can be inherited in an autosomal dominant or autosomal recessive pattern.
  6. Autosomal dominant HCA is caused by mutations in a single copy of a gene, while autosomal recessive HCA is caused by mutations in both copies of a gene.
  7. There is no cure for HCA, but treatments can help to manage the symptoms and improve quality of life.
  8. HCA can progress at different rates, and some individuals may experience only mild symptoms, while others may become severely disabled.
  9. HCA can be associated with other neurological disorders, such as epilepsy and intellectual disability.
  10. HCA is a rare disorder, affecting approximately 1 in 100,000 people worldwide.

FAQs About the word hereditary cerebellar ataxia

nervous disorder of late childhood and early adulthood; characterized by ataxic gait and hesitating or explosive speech and nystagmus

No synonyms found.

No antonyms found.

Hereditary cerebellar ataxia (HCA) is a genetic disorder characterized by progressive degeneration of the cerebellum.

HCA can affect individuals at any age, with the onset of symptoms typically occurring in the third or fourth decade of life.

The most common symptoms of HCA include difficulty with balance and coordination, slurred speech, and involuntary eye movements.

HCA is caused by mutations in genes that encode proteins essential for proper cerebellar function.