AgeX and UCI to Research Huntington Disease Therapies
AgeX Therapeutics will collaborate with neurology researchers at the University of California, Irvine, (UCI) to research... Read More
AgeX Therapeutics will collaborate with neurology researchers at the University of California, Irvine, (UCI) to research... Read More
Fabry disease is an inherited disorder caused by a mutation found on the X chromosome. Inadequate functioning of the lys... Read More
In a February 10, 2020 press release about clinical data of pegunigalsidase alfa for the treatment of Fabry disease, Pro... Read More
What Is Fabry Disease? Fabry disease is an inherited multi-organ metabolic disorder that is caused by a build-up of a t... Read More
What is Neurofibromatosis? Neurofibromatosis (NF) is a genetic disorder that affects the nervous system. It can affect t... Read More
Huntington's disease (HD) is a rare progressive genetic disorder in which nerve cells in certain parts of the brain dege... Read More
La enfermedad de Huntington (EH) es un trastorno genético progresivo y poco común, en el que las células nerviosas, en c... Read More
What is 22q Deletion Syndrome? 22q Deletion Syndrome is the most common chromosome deletion syndrome, and is roughly as... Read More
¿Qué es el síndrome de deleción 22q? El síndrome de deleción 22q es el síndrome de deleción cromosómica más común, y es... Read More
Disclaimer: One of the sources cited in this article is Dr. Mauricio De Castro, Associate Director for the Air Force Med... Read More
What Is Fragile X Syndrome? Fragile X Syndrome (FXS) is a genetic condition that causes several developmental problems i... Read More
What is Duchenne Muscular Dystrophy? Duchenne muscular dystrophy (DMD) is the most common childhood onset form of muscul... Read More
TANGO2 Disease Dr. Seema Lalani, a clinical geneticist at Texas Children's Hospital, and a faculty member in the Departm... Read More
What is 5p Minus Syndrome? In 1963, a French physician, Dr. Lejeune first described 5p- syndrome. He originally named t... Read More
Interviewees Lauren Giannetti Sferrazza is a certified genetic counselor who works at Myriad Genetics as a Regional Medi... Read More
What is Charcot Marie Tooth Disease (CMT)? Charcot-Marie-Tooth disease (CMT) is one of a group of disorders that cause d... Read More
What is Angelman Syndrome? In 1965, English physician Dr. Harry Angelman first described three children with signs that... Read More
Interviews Dr. Oliver Adunka, an otolaryngologist specializing in Neurotology. that deals with disorders of the ear, hea... Read More
Interviews with Meg Hafner, a St. Louis genetic counselor and special advisor for the CHARGE Syndrome Foundation. She h... Read More
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