Prader-Willi syndrome is a congenital (present from birth) disease that involves obesity, decreased muscle tone, decreased mental capacity, and sex glands that produce little or no hormones.
Prader-Willi syndrome is caused by a gene missing on part of chromosome 15. Normally, your parents each pass down a copy of this chromosome. Most patients with Prader-Willi syndrome are missing the genetic material on part of the father's chromosome. The...
Read moreIt doesn't matter what virus, disease, handicap or challenge people face, there is a constant medical and scientific quest to find a cure... Read more »
Fear, it seems, runs rampant in families with a loved one affected by Alzheimer's disease. Those caring for a declining parent or... Read more »
Reader's Question: My mother and father had skin cancer. Does this mean I will inherit skin cancer from my parents? Dr. Berman's... Read more »
When researchers, observers, and hypothesizers begin to make connections, it can become very interesting. I recently came across listings... Read more »
A study of 9 children who have inherited a severe form of early-onset colitis may help unlock secrets to IBD. Researchers found mutations of two... Read more »
According to new research, people who have the inherited skin disorder known as Gorlin syndrome may be able to reduce their risk of developing skin... Read more »
Source: Medifocus Guidebook on: Restless Legs Syndrome
The first description of Restless Legs Syndrome (RLS) was provided in 1685 by Sir Thomas Willis. The current name for this sleep and movement... Read more »
Source: ADAM Encyclopedia
Alstrm syndrome is a very rare inherited disease that can lead to blindness, deafness, diabetes, and obesity.Causes, incidence, and risk... Read more »
Source: ADAM Encyclopedia
Riley-Day syndrome is an inherited disorder that affects the development and function of nerves throughout the body.Alternative NamesFamilial... Read more »