Hereditary Spastic Paraplegia Publication Trend The graph below shows the total number of publications each year in Hereditary Spastic Paraplegia.

In what experts are calling a “dream come true,” scientists used a recent biochemical discovery to help an 8-year-old boy ...

The approval of Andembry is for use in adult and pediatric patients aged 12 years and older and is self-administered with once-monthly dosing delivered in 15 seconds or less via an autoinjector ...

Mutations in DDHD2 are linked to a type of hereditary spastic paraplegia, a neurological condition that causes progressive stiffness and weakness in the legs, in addition to cognitive deficits.

Peers supported an amendment to the House of Lords (Hereditary Peers) Bill that would instead see a gradual reduction of bloodline peers.

However, because spastic paraparesis has only been described in two of four families with Δ9 variations and because it may also be associated with other PS1 missense mutations 3, the specific ...

Parkinson’s disease is a neurodegenerative disorder that affects the nervous system. Studies show that some cases are caused by genetic mutations, but hereditary causes are rare.

Living with hereditary angioedema (HAE) can be challenging. You may have to pay close attention to potential triggers or follow a strict medication regimen in order to avoid attacks.

The Genetics of Hereditary Retinopathies and Optic Neuropathies Alessandro Iannaccone, MD, MS Disclosures Compr Ophthalmol Update. 2005;6 (1):39-62.

Iron-refractory iron deficiency anemia (IRIDA) is a genetic form of anemia. Learn about the causes, symptoms, diagnosis, and treatment of this condition.

The Whitrod family launched Genetic Cures for Kids in the hopes of finding a treatment for their daughter with hereditary ...