Prader

Pra·der

(pră'dĕr),
Andrea, Swiss pediatrician, *1919. See: Prader-Willi syndrome.
References in periodicals archive ?
The Northstar Centre supports as many as 25 adults, who have a range of disabilities including Down's Syndrome, Fragile X Syndrome and Prader Willi Syndrome.
Individuals who have intellectual impairments either in isolation or as part of another disability such as Down Syndrome, Autism, Pervasive Developmental Disorder, Mild Mental Retardation, Tourette Syndrome, Cerebral Palsy, Prader Willi Syndrome or others, and are 14 years old and above would be "really invaluable in helping us raise awareness of strategies medical students could use to enhance communication with these individuals", the school said.
Elevated plasma ghrelin levels in Prader Willi syndrome.
It was first described in 1956 by Swiss doctors, Prof A Prader, Dr A Labhart and Dr H Willi, who recognised the condition as having unique and clearly definable features.
Justin, of Coalburn, Lanarkshire, was born with the rare genetic disorder Prader Willi syndrome, which leaves him unable to walk or breathe on his own.
Last year''s title went to Austrian Clemens Prader, but this is the first time the event has been part of the tour since 1997.
He suffers from Prader Willi syndrome, which means he never feels full and can't stop eating.
Cummings examined people with Prader Willi and found their blood ghrelin levels to be the highest ever recorded in humans: 4.
ended up with [genitalia rated as] Prader 1, which is normal, or Prader 2 at the most," Dr.
Contractor name : ASSOCIATION D~ENTREPRISES COLAS SUISSE SA - PRADER LOSINGER SA
This constellation was first described by Down (1887) and at a later date by Prader, Labhart, and Willi (1956).
Justin, five, who lives in nearby Coalburn, has Prader Willi syndrome - a severe genetic disorder which means he regularly suffers life-threatening seizures.