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"Huntington's" chorea
- ... chorea Huntington chronic progressive hereditary chorea Huntington disease Huntington's chorea Genetic Testing Registry: Juvenile Huntington disease Genetic Testing ...
- As its name suggests, a Huntington's disease-like (HDL) syndrome is a condition that resembles Huntington's disease. Researchers have described four HDL ...
- ... 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 ...
- ... For some conditions, such as the neurological condition Huntington's disease , signs and symptoms occur later in life, typically ...
- ... no history of the disorder in their family. Huntington's disease , Marfan syndrome Autosomal recessive In autosomal recessive inheritance , ...
- ... genetic disorders of the nervous system, such as Huntington's disease , myotonic dystrophy , and fragile X syndrome . Anticipation typically ...
