A child with a rare genetic disease that affects mitochondria is the first person to receive a new experimental treatment for ...

Microglia replacement therapy helps treat people with a rare genetic condition called ALSP, suggesting the approach could ...

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a progressive neurological disease with an ...

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a progressive neurological disease with an ...

The value of a recent biochemical discovery can be seen in the case of an 8-year-old boy who was playing typical sports in ...

For those who haven’t entered the valley of middle age, a CAC is a specialized CT scan that looks for calcium deposits in the ...

An 8-year-old boy, wheelchair-bound due to a rare genetic disease, HPDL deficiency, regained his mobility through an ...

Among members of the Richardson family who carry a mutation in the PSEN1 gene, the average age when symptoms start is 39.

PROVIDENCE – The Rhode Island Department of Health is alerting the public throgh a press release that a stray cat found in the area of Newell Court in Coventry tested ...

The World Heath Organisation has warned people of a 'fatal disease' being spread by mosquitoes in two neighbourhoods in Spain ...