It was discovered in 1863 by a Swiss Doctor named Labhart
Andrea Prader, Heinrich Willi, Alexis Labhart, Andrew Ziegler and Guido Franconi were first to observe Prader Willi Syndrome in 1956.
no
no
A person inherits Prader-Willi syndrome from the paternal chromosomes. This basically means that you had seven genes that were unexpressed.
Yes he does.
There are no guidelines for preventing Prader-Willi syndrome. Prader-Willi Syndrome is a result of a genetic "error" that occurs at conception therefore there is nothing that can be done to prevent it. Liken it to not being able to prevent hair color or eye color....two things that occur as a result of DNA at conception.
1 in 15,000 people have it
Prader-Willi Syndrome
According to the research I've done, Prader-Willi Syndrome is rarely a result of translocation, but it is a possibility. Translocation in this syndrome results in an inactivation of genes on the paternal chromosome 15.
According to Wikipeda, the incidence of Prader-Willi Syndrome is between 1 in 10,000 and 1 in 25,000 live births .
Chromosome 15q partial deletion is the name for this syndrome.
It was named after the two doctors who diagnosed it