Cause of Prader Willi Syndrome

Prader-Willi syndrome - Prader-Willi syndrome is a genetic disorder in which seven genes (or some subset thereof) on chromosome 15 are missing or unexpressed (chromosome 15q partial deletion). It was identified in 1956 by Andrea Prader, Heinrich Willi, Alexis Labhart, and Guido Fanconi of Switzerland.

Willi Willi National Park - Willi Willi is a national park in New South Wales (Australia), 325 km northeast of Sydney.

Kabuki syndrome - Kabuki syndrome, also previously known as Kabuki makeup syndrome or Niikawa Kuroki Syndrome, is a very rare pediatric congenital disorder. It's named Kabuki Syndrome because of the facial resemblance of affected individuals with white Kabuki makeup, the name Niikawa-Kuroki Syndrome relates to the two Japanese doctors who first described this syndrome.

Hallermann-Streiff syndrome - The Hallermann-Streiff syndrome (also known as the François Dyscephalic Syndrome, Hallermann-Streiff-François syndrome, Oculomandibulodyscephaly with hypotrichosis and the Oculomandibulofacial Syndrome) is a disorder that effects the body's stature, head structure and hair growth. Patients with this syndrome are shorter than the average person and may not develop hair in many places, including in the facial, leg and pubic areas.

causeofpraderwillisyndrome

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