Prader–Willi syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. In newborns, symptoms include...

first described the syndrome in 1965. An older term, happy puppet syndrome, is generally considered pejorative. Prader–Willi syndrome is a separate condition...

deletion syndromes include 5p-Deletion (cri du chat syndrome), 4p-Deletion (Wolf–Hirschhorn syndrome), Prader–Willi syndrome, and Angelman syndrome. The chromosomal...

protein MIR9-3 host gene NIPA2: encoding protein Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 NUSAP1: encoding protein Nucleolar and spindle...

of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome". Human Genetics. 116 (3): 228–30. doi:10.1007/s00439-004-1219-2...

maladaptive, obsessive-compulsive, affiliative and satiety behaviors in Prader–Willi syndrome". Bialik started her career as a child actress in the late 1980s...

snoRNA SNORD116 has been shown to be the primary cause of Prader–Willi syndrome. Prader–Willi is a developmental disorder associated with over-eating and...

Turner syndrome (TS), also known as 45,X, or 45,X0, is a genetic disorder in which a female is partially or completely missing an X chromosome (sex chromosome...

There may be an association with Prader–Willi syndrome, and around a third of individuals with Ehlers–Danlos syndrome may have them. Risk factors include...

including Angelman Syndrome, Prader-Willi Syndrome, and DiGeorge Syndrome. Some syndromes, including Angelman syndrome and Prader-Willi syndrome, are associated...

2023-02-21. "Prader-Willi syndrome: MedlinePlus Genetics". medlineplus.gov. Retrieved 2021-06-24. "What Is Prader-Willi Syndrome?". Prader-Willi Syndrome Association...

diseases, e.g., Graves' disease, and it has also been noted in Prader–Willi syndrome and other genetic conditions caused by chromosomal anomalies. It...

Andrea Prader (December 23, 1919 – June 3, 2001) was a Swiss scientist, physician, and pediatric endocrinologist. He co-discovered Prader–Willi syndrome and...

Prader may refer to: Andrea Prader (1919–2001) Prader–Willi syndrome Prader scale This disambiguation page lists articles associated with the title Prader...

Down syndrome or Down's syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome...

specific genes (e.g., GHRHR, GH1) congenital diseases such as Prader-Willi syndrome, Turner syndrome, or short-stature homeobox gene deficiency congenital malformations...

inheritance patterns including Prader-Willi/Angelman Syndromes, Beckwith-Wiedemann Syndrome, and Silver-Russell Syndrome. Disorders of imprinting are thought...

for her large size and weight, now thought to be the result of Prader–Willi Syndrome. Vallejo was born in the small village of Merindad de Montija, Burgos...

Heinrich Willi (4 March 1900 – 16 February 1971) was a Swiss pediatrician who specialised in neonatology and co-discovered Prader–Willi syndrome with Andrea...

RV, Turner S, Ledbetter DH, Martin CL (1993). "17q12 Recurrent Deletion Syndrome". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya...

Potocki–Shaffer syndrome Potter sequence Prader–Willi syndrome Pre-excitation syndrome Precordial catch syndrome Premenstrual syndrome Presumed ocular...

diseases involving genomic imprinting include Angelman, Prader–Willi, and Beckwith–Wiedemann syndromes. Methylation defects have also been associated with...

syndrome and Prader–Willi syndrome – both can be produced by the same genetic mutation, chromosome 15q partial deletion, and the particular syndrome that...

number of other genetic disorders, including Klinefelter's Syndrome and Prader-Willi syndrome, as well as other multiple malformation disorders. The degree...

flattened or smooth philtrum may be a symptom of fetal alcohol syndrome or Prader–Willi syndrome. A study of boys diagnosed with autism spectrum disorders...

Noonan syndrome Neurofibromatosis Patau syndrome a.k.a. trisomy 13 Pituitary dwarfism/growth hormone deficiency(in adults) Prader–Willi syndrome Rett syndrome...

Urban–Rogers–Meyer syndrome, also known as Prader–Willi habitus, osteopenia, and camptodactyly or Urban syndrome, is an extremely rare inherited congenital...

is an experimental antiobesity drug being tested in people with Prader-Willi syndrome and monogenic obesity caused by mutations in the SH2B1, PCSK1, or...

feature in several syndromes, such as Prader–Willi syndrome, Bardet–Biedl syndrome, Cohen syndrome, and MOMO syndrome. (The term "non-syndromic obesity" is sometimes...

ghrelin does not contribute to obesity, except in the cases of Prader–Willi syndrome-induced obesity, where high ghrelin levels are correlated with increased...