• Thumbnail for Prader–Willi syndrome
    PraderWilli syndrome (PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. In newborns, symptoms include...
    39 KB (4,067 words) - 00:27, 29 January 2025
  • Thumbnail for Angelman syndrome
    first described the syndrome in 1965. An older term, happy puppet syndrome, is generally considered pejorative. PraderWilli syndrome is a separate condition...
    39 KB (4,147 words) - 10:02, 1 February 2025
  • deletion syndromes include 5p-Deletion (cri du chat syndrome), 4p-Deletion (Wolf–Hirschhorn syndrome), PraderWilli syndrome, and Angelman syndrome. The chromosomal...
    9 KB (1,128 words) - 14:12, 9 January 2025
  • Thumbnail for Williams syndrome
    "Refining Behavioral Phenotypes: Personality—Motivation in Williams and Prader-Willi Syndromes". American Journal on Mental Retardation. 104 (2): 158–69. doi:10...
    52 KB (5,774 words) - 20:22, 29 January 2025
  • Thumbnail for Down syndrome
    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...
    148 KB (14,788 words) - 14:50, 31 January 2025
  • Thumbnail for Turner syndrome
    Turner syndrome (TS), commonly known as 45,X, or 45,X0, is a chromosomal disorder in which female cells have only one X chromosome instead of two, or are...
    80 KB (9,433 words) - 15:08, 31 January 2025
  • Eventually, this disorder was ruled distinct from a syndrome presented by Prader and Willi (Prader-Willi syndrome) because of its mode of inheritance, gynecomastia...
    18 KB (2,206 words) - 09:43, 2 January 2025
  • Thumbnail for Silver–Russell syndrome
    imprinting disorders (e.g. PraderWilli syndrome, Angelman syndrome, and Beckwith–Wiedemann syndrome), Silver–Russell syndrome may be associated with the...
    15 KB (1,649 words) - 02:17, 28 January 2025
  • Thumbnail for Börjeson–Forssman–Lehmann syndrome
    include PraderWilli syndrome, Coffin–Lowry syndrome, Klinefelter syndrome, Wilson–Turner syndrome, Bardet–Biedl syndrome, Smith–Fineman–Myers syndrome (Chudley-Lowry...
    8 KB (716 words) - 16:23, 14 November 2023
  • diseases, e.g., Graves' disease, and it has also been noted in PraderWilli syndrome and other genetic conditions caused by chromosomal anomalies. It...
    6 KB (528 words) - 00:13, 21 October 2024
  • hydroxymethyltransferase Charcot-Marie-Tooth disease Potocki-Lupski syndrome Prader-Willi syndrome Bi, W; Yan, J; Stankiewicz, P; Park, SS; Walz, K; Boerkoel,...
    13 KB (1,525 words) - 03:55, 23 January 2025
  • Thumbnail for Austin de Lone
    Special Housing Project, a residential facility for people with Prader-Willi Syndrome, which de Lone's son Richard is afflicted with. As part of the 2007 event...
    12 KB (1,125 words) - 21:41, 20 January 2025
  • Potocki–Shaffer syndrome Potter sequence PraderWilli syndrome Pre-excitation syndrome Precordial catch syndrome Premenstrual syndrome Presumed ocular...
    42 KB (4,068 words) - 16:56, 1 November 2024
  • Thumbnail for Eugenia Martínez Vallejo
    the result of PraderWilli Syndrome. Vallejo was born in the small village of Merindad de Montija, Burgos, Spain in 1674, to Antonia de la Bodega and...
    8 KB (654 words) - 03:54, 25 November 2024
  • Thumbnail for Hypotelorism
    as Patau syndrome, as well as hereditary neuralgic amyotrophy. It can also be associated with fragile X syndrome and PraderWilli syndrome. Metopic synostosis...
    3 KB (140 words) - 07:00, 15 September 2023
  • Thumbnail for 1p36 deletion syndrome
    1p36 deletion syndrome is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures...
    12 KB (1,057 words) - 03:53, 8 October 2024
  • Thumbnail for Diazoxide
    is an experimental antiobesity drug being tested in people with Prader-Willi syndrome and monogenic obesity caused by mutations in the SH2B1, PCSK1, or...
    11 KB (892 words) - 00:34, 13 January 2025
  • Noonan syndrome Neurofibromatosis Patau syndrome a.k.a. trisomy 13 Pituitary dwarfism/growth hormone deficiency(in adults) PURA syndrome PraderWilli syndrome...
    22 KB (2,496 words) - 09:21, 2 January 2025
  • Pierre Robin syndrome Poland syndrome Polydactyly Polymelia Polysyndactyly PraderWilli syndrome Proteus syndrome Prune belly syndrome Radial aplasia...
    4 KB (357 words) - 13:01, 28 September 2024
  • Medicine, specializing in Fragile X syndrome, Prader-Willi syndrome, and in research on the relationship of Fragile X syndrome to other conditions, including...
    2 KB (172 words) - 14:52, 6 October 2024
  • Thumbnail for Deletion (genetics)
    including Angelman Syndrome, Prader-Willi Syndrome, and DiGeorge Syndrome. Some syndromes, including Angelman syndrome and Prader-Willi syndrome, are associated...
    14 KB (1,537 words) - 02:33, 14 May 2024
  • Thumbnail for Excoriation disorder
    disabilities; for example, PraderWilli syndrome and Smith–Magenis syndrome. Studies have shown that 85% of people with PraderWilli syndrome also engage in skin-picking...
    44 KB (5,376 words) - 00:39, 28 January 2025
  • Thumbnail for Non-coding RNA
    snoRNA SNORD116 has been shown to be the primary cause of PraderWilli syndrome. PraderWilli is a developmental disorder associated with over-eating and...
    67 KB (7,178 words) - 04:34, 29 October 2024
  • diseases involving genomic imprinting include Angelman, PraderWilli, and Beckwith–Wiedemann syndromes. Methylation defects have also been associated with...
    57 KB (6,847 words) - 09:02, 12 December 2024
  • fall under a prevalence rate of 4-6%. For children diagnosed with Prader-Willi syndrome (PWS), CSA is more common and can occur in up to 53% of cases. Research...
    32 KB (3,918 words) - 18:09, 12 January 2025
  • Thumbnail for MKRN3
    allele. Disruption of the imprinting at this locus may contribute to PraderWilli syndrome. An antisense RNA of unknown function has been found overlapping...
    4 KB (618 words) - 02:01, 4 March 2023
  • Post-polio syndrome Postherpetic neuralgia Posttraumatic stress disorder Postural hypotension Postural orthostatic tachycardia syndrome PraderWilli syndrome Primary...
    13 KB (1,143 words) - 17:54, 21 January 2025
  • Thumbnail for Isodicentric 15
    for the symptoms of idic(15) syndrome is the critical PWS/AS-region named after the Prader-Willi and/or Angelman syndromes.[citation needed] For more than...
    20 KB (2,370 words) - 04:33, 7 July 2024
  • contributions to the discovery of the genetic causes of PraderWilli and Miller–Dieker syndromes. His research has focused on developing and applying technologies...
    5 KB (513 words) - 14:14, 27 July 2024
  • Thumbnail for Appetite
    genetics on a chromosomal scale, shown by the 1950s discovery of PraderWilli syndrome, a type of obesity caused by chromosome alterations. Additionally...
    14 KB (1,553 words) - 16:34, 15 January 2025