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"Huntington's" chorea
- ... The inherited variant (also called mutation) that causes Huntington's disease is known as a CAG trinucleotide repeat expansion. ... CAG segment in the HTT gene. People with Huntington's disease have 36 to more than 120 CAG repeats. ...
- ... cause signs and symptoms that resemble those of Huntington's disease, including uncontrolled movements, emotional problems, and loss of thinking ability. Researchers have named this condition Huntington's disease-like 2 (HDL2).The variant associated with HDL2 ...
- ... to cause a progressive brain disorder known as Huntington's disease-like 4 (HDL4) or spinocerebellar ataxia type 17 ( ... whose signs and symptoms closely resembled those of Huntington's disease, including uncontrolled movements, emotional problems, and loss of ...
- ... cause signs and symptoms that resemble those of Huntington's disease, including uncontrolled movements, emotional problems, and loss of ... Researchers have proposed that this condition be called Huntington's disease-like 1 (HDL1).The PRNP gene variants associated ...