Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jeanne M. Hanchett"'
Publikováno v:
Clinical Genetics. 26:161-163
Reports of Black females with Prader-Willi have been rare. This communication describes two Black females with Prader-Willi syndrome. Chromosome analysis revealed a small deletion of the proximal portion of a chromosome 15 in one case and apparently
Publikováno v:
American Journal of Medical Genetics. 66:403-412
We report on our findings of 4 patients with mosaicism for a deletion of chromosome 15, most commonly associated with Prader-Willi syndrome (PWS). We examined a series of typical and atypical PWS patients in order to identify cytogenetically undetect
Autor:
Suzanne B. Cassidy, Merlin G. Butler, Frank Greenberg, Barbara Y. Whitman, Louise R. Greenswag, Vanja A. Holm, Jeanne M. Hanchett
Publikováno v:
Pediatrics. 91:398-402
The diagnosis of Prader-Willi syndrome (PWS) is based on clinical findings that change with age. Hypotonia is prominent in infancy. Obesity, mild mental retardation or learning disability, and behavior problems, especially in association with food an
Publikováno v:
Management of Prader-Willi Syndrome ISBN: 9780387253978
Prader-Willi syndrome (PWS) is a complex genetic condition characterized by a range of mental and physical fi ndings, with obesity being the most signifi cant health problem. PWS is considered to be the most common genetically identifi ed cause of li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d968c599fabfb4ae4a02a2bcb40f91ba
https://doi.org/10.1007/978-0-387-33536-0_1
https://doi.org/10.1007/978-0-387-33536-0_1
Publikováno v:
Pediatrics. 97:265-267
Individuals with Prader-Willi syndrome manifest severe skin picking behavior. We report three patients with this syndrome in whom an extension of this behavior to rectal picking resulted in significant lower gastrointestinal bleeding and anorectal di
Autor:
William G. North, Jeanne M. Hanchett, George M. Anderson, Claire McConaha, James F. Leckman, Andrés Martin, Walter M Kaye, Matthew W. State
Publikováno v:
Biological psychiatry. 44(12)
Background: Prader–Willi syndrome (PWS) is a genetic disorder characterized by mental retardation, appetite dysregulation, and a high risk for obsessive–compulsive disorder (OCD). Microscopic abnormalities of the hypothalamus have been described
Publikováno v:
New England Journal of Medicine. 350:1470-1471
Autor:
Beate V. Maier, Jeanne M. Hanchett
Publikováno v:
Management of Prader-Willi Syndrome ISBN: 9780387952055
Management of Prader-Willi Syndrome
Management of Prader-Willi Syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b88855c76a48389babcb41eba5fde0c3
https://doi.org/10.1007/978-1-4615-7384-5_17
https://doi.org/10.1007/978-1-4615-7384-5_17
Publikováno v:
Prader-Willi Syndrome ISBN: 9783642842856
Prader-Willi Syndrome (PWS) was identified in 1956 (Prader et al, 1956) and has been reported to occur in all racial groups (Golden et al, 1984; Ikeda et al, 1973). Clinical diagnosis is based on the presence of hypotonia in infancy, obesity occurrin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a72832d00052d66f98888f35bfc2a7c7
https://doi.org/10.1007/978-3-642-84283-2_17
https://doi.org/10.1007/978-3-642-84283-2_17
Publikováno v:
American Journal of Medical Genetics. 90:177-177