Huntington's disease
ICD-10 G10
Definition
Huntington's disease (HD) is an inherited disease that causes certain nerve cells in the brain to waste away. People are born with the defective gene, but symptoms usually don't appear until middle age. Early symptoms of HD may include uncontrolled movements, clumsiness, and balance problems. Later, HD can take away the ability to walk, talk, and swallow. Some people stop recognizing family members. Others are aware of their environment and are able to express emotions. If one of your parents has Huntington's disease, you have a 50% chance of getting it. A blood test can tell you if have the HD gene and will develop the disease. Genetic counseling can help you weigh the risks and benefits of taking the test. There is no cure. Medicines can help manage some of the symptoms, but cannot slow down or stop the disease. NIH: National Institute of Neurological Disorders and Stroke
Rare disease
Related medicines
- BRANAPLAM HYDROCHLORIDE
- VOTOPLAM
- MAVOGLURANT
- BRANAPLAM
- TETRABENAZINEUS label →
- CANNABIDIOLUS label →
- GSK-356278
- LEXANERSEN SODIUM
- VALBENAZINEUS label →
- BEVANTOLOL HYDROCHLORIDE
- RILUZOLEUS label →
- ACETYLCYSTEINEUS label →
Disease
- G00Bacterial meningitis, not elsewhere classified
- G01tuberculous meningitis
- G02Meningitis in other infectious and parasitic diseases classified elsewhere
- G03Meningitis due to other and unspecified causes
- G04myelitis
- G05encephalitis
- G06Intracranial and intraspinal abscess and granuloma
- G07Intracranial and intraspinal abscess and granuloma in diseases classified elsewhere
- G08Intracranial and intraspinal phlebitis and thrombophlebitis
- G09Sequelae of inflammatory diseases of central nervous system
- G11Hereditary ataxia
- G12spinal muscular atrophies