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Genetic Disorders
Huntington's disease is an inherited neurological illness causing involuntary movements, severe emotional disturbance and cognitive decline.
… Huntington's disease is an inherited neurological illness causing … severe emotional disturbance and cognitive decline. … Huntington's disease (HD) is an inherited neurological …
Educational Resources
Huntington's disease is an inherited disease characterized by the progressive loss of brain and muscle function.
… Huntington's Disease … Huntington's disease is an inherited disease characterized by …
Talking Glossary
La enfermedad de Huntington es un trastorno hereditario raro que se asocia con la pérdida progresiva de la función cerebral y muscular.
… Enfermedad de Huntington … La enfermedad de Huntington es un trastorno … progresiva de la función cerebral y muscular. … Huntington’s disease is a rare inherited disorder associated with the …
For Patients and Families
A rare disease is generally considered to be a disease that affects fewer than 200,000 people in the United States at any given time.
… A rare disease is generally considered to be a disease that affects … digestive systems (See: Learning About Cystic Fibrosis ); Huntington's disease, which affects the brain and nervous system (See: …
News Release
NHGRI will highlight rare disease research that benefits affected patients and provides insights into more common disorders on Rare Disease Day.
… Institute (NHGRI) researchers are highlighting rare disease research that benefits affected patients and also … research updates at the February 27 event. In NHGRI's Medical Genetics Branch , for example, Ellen Sidransky, … the rare Gaucher disease and the more common Parkinson's disease. While patients with Gaucher disease are at …
Educational Resources
A complex disease is caused by the interaction of multiple genes and environmental factors.
… Complex Disease … A complex disease is caused by the interaction of multiple genes and environmental factors. … Genes, Cancer, Heart Disease, Gene-environment Interactions … A complex disease …
15 Ways Genomics Influences Our World
Genomics is ending diagnostic odysseys for patients with rare diseases.
… trying to find the root cause for their family member's rare disorder. It is difficult to overstate the relief that … a mutation in each copy of a gene called  NGLY1 . Bertrand's mutations meant that he had no functioning copy of this … identification of at least 15 other children with the same disease, and the establishment of the  NGLY1 Foundation  to …
For Patients and Families
The Genetic and Rare Diseases Information Center helps people find useful information about genetic and rare diseases.
… and teachers who work with people with a genetic or rare disease. Even scientists who are studying a genetic or rare disease and who need information for their research have … Contact Us On the GARD website. Fax: (301) 251-4911 By U.S. Mail: The Genetic and Rare Diseases Information Center …
Clinical Research
The Undiagnosed Diseases Program provide answers to patients with mysterious conditions that have long eluded diagnosis.
… Diseases Program (UDP) is part of the Undiagnosed Disease Network (UDN), an NIH Common Fund initiative that … study following careful application review by the program's medical team. In general, it takes 8 to 12 weeks for the … expert consultations provided for free at one of the world's largest medical research institutes. The patient is …
Genetic Disorders
Charcot-Marie-Tooth disease is an inherited neurological disease characterized by a slowly progressive degeneration of the muscles and loss of sensation.
… Charcot-Marie-Tooth disease (CMT) is an inherited neurological disease characterized by a slowly progressive degeneration of … two defective forms of the gene implicated in Lou Gehrig's disease are known to interact with a GARS  family member. …