Marcus Gunn Syndrome, or Marcus Gunn jaw winking ptosis, is a rare congenital disorder that presents as a droopy eyelid ...

Purpose: To evaluate the cochlear function of parents of individuals with autosomal recessive gene Gap Junction Protein Beta-2 hearing loss by ultra-high frequencies distortion-product otoacoustic ...

Spinal muscular atrophy (SMA) is a rare genetic condition mostly caused by inherited mutations in the SMN1 gene, although rarer forms of the disease can arise due to mutations in a number of other ...

Most cases of hemophilia — a group of rare bleeding disorders — are genetic, arising when children directly inherit disease-causing mutations from their biological parents. These mutations result in ...

Cystic fibrosis represents one of the most common inherited genetic disorders affecting people of European descent, touching the lives of approximately 30,000 individuals in the United States alone.

Familial Alzheimer’s disease (FAD) is a rare type of Alzheimer’s disease (AD) caused by a gene mutation passed down through families. With FAD, symptoms start when you’re young. You may have symptoms ...

According to Science Alert, neuroscientists from Johns Hopkins University have recently discovered a new treatment for Parkinson's disease using an FDA-approved cancer drug. A recent study published ...

As record numbers of baby boomers reach retirement age, I keep coming across articles and studies about living inheritances. When structured correctly, a living inheritance (also known as an ...

Biological inheritance vector illustration infographic. Biology... Biological inheritance vector illustration infographic. Educational biology scheme with parents, son and daughter. Carrier father, ...

Retinitis pigmentosa (RP) is an eye condition that can be genetic. In this way, people usually need to inherit two copies of a genetic variation that causes RP, one coming from each parent. RP may ...