Search Results

Facet (Page)

Content Formats

1 - 10 of 1133

Genetic Disorders

Gaucher disease is an autosomal recessive inherited disorder of metabolism where a type of fat (lipid) called glucocerebroside cannot be adequately degraded.

… Gaucher disease is an autosomal recessive inherited disorder of … called glucocerebroside cannot be adequately degraded. … Gaucher disease is an autosomal recessive inherited disorder of …

News Release

Researchers make advance in possible treatments for Gaucher, Parkinson's diseases

NIH researchers have identified and tested a molecule that shows promise as a possible treatment for Gaucher disease and Parkinson's disease.

… that shows promise as a possible treatment for the rare Gaucher disease and the more common Parkinson's disease. Ellen … of Neuroscience . … "Until now, drugs used to treat Gaucher disease have not been able to enter the brain and …

News Release

Mouse model for rare genetic disease advances understanding of Parkinson's

NHGRI researchers are studying the link between Parkinson's disease, and a rare disorder, Gaucher disease, by cross-breeding mice with the disease mutations.

… the puzzling link between a common disorder, Parkinson's disease, and a rare disorder, Gaucher disease, by cross-breeding mice to carry human … Genetics and Metabolism . … A single mutation in the Gaucher disease gene, GBA1, is frequently found in patients …

News Release

NIH researchers use a new cell model of a rare disease to develop therapeutic compounds

A team from the NIH has surmounted a major obstacle to testing potential drug therapies for a rare, genetic condition called Gaucher disease.

… drug therapies for a rare, genetic condition called Gaucher disease. Researchers from the National Human Genome Research … has successfully corrected the malfunctioning cells. … Gaucher disease is an inherited condition caused by …

Clinical Research

Gaucher Disease Clinical Studies at NIH

In the late 90’s and early 2000’s, scientists at the NIH highlighted an increased incidence of Parkinson disease among patients with GD and their families.

… Gaucher disease (GD) is a rare (autosomal recessive) genetic … and neurological manifestations seen in patients with Gaucher disease. The gene coding for the enzyme glucocerebrosidase is …

News Release

Rare disease research may provide insights into common diseases

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 … have been probing the connection between the rare Gaucher disease and the more common Parkinson's disease. While patients with Gaucher disease are at increased risk for Parkinson's …

Staff

Ellen Sidransky, M.D.

Dr. Ellen Sidransky is a pediatrician and clinical geneticist in the Medical Genetics Branch at the National Human Genome Research Institute.

… includes both clinical and basic research aspects of Gaucher disease and Parkinson's disease, and her group first … in "simple" Mendelian disorders, the association between Gaucher disease and parkinsonism and the development of small …

For Patients and Families

Rare Diseases FAQ

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 fewer than 200,000 people in the United … a role in rare diseases. Such factors may directly cause disease, or interact with genetic factors to cause or …

Educational Resources

Complex Disease

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

Rare Genetic Diseases

Genomics is ending diagnostic odysseys for patients with rare diseases.

… identification of at least 15 other children with the same disease, and the establishment of the NGLY1 Foundation to support research about the disease and pursue possible treatments. In 2015, Matt was one … sequencing can transform the life of someone with a rare disease comes from Sonia Vallabh and Eric Minikel . After a …