APAKAH MAKSUD PRADER-WILLI SYNDROME dalam CORSICA?
Sindrom Prader-Willi
Sindrom Prader-Willi (disingkat PWS) adalah gangguan genetik yang jarang berlaku di mana tujuh gen (atau beberapa subsetnya) pada kromosom 15 (q 11-13) dipadam atau tidak dinyatakan (kromosom 15q penghapusan separa) kromosom. Ia pertama kali digambarkan pada tahun 1956 oleh Andrea Prader (1919-2001), Heinrich Willi (1900-1971), Alexis Labhart (1916-1994)), Andrew Ziegler, dan Guido Fanconi dari Switzerland. Ciri-ciri PWS adalah "nada otot yang rendah, kedudukan pendek, perkembangan seksual yang tidak lengkap, ketidakupayaan kognitif, tingkah laku masalah, dan perasaan kelaparan yang kronik yang boleh membawa kepada kegunaan yang berlebihan dan obesiti yang mengancam nyawa." Insiden PWS adalah antara 1 dalam 25,000 dan 1 dalam 10,000 kelahiran hidup. Asal mula bahan genetik yang terjejas dalam sindrom adalah penting kerana rantau tertentu kromosom 15 yang terlibat tertakluk kepada ibu bapa asal mencetak, bermakna bahawa untuk beberapa gen di rantau ini hanya satu salinan gen dinyatakan sementara yang lain disenyapkan melalui pencetakan.
Definisi Prader-Willi syndrome dalam kamus Corsica
Takrif sindrom Prader-Willi dalam kamus adalah keadaan kongenital yang ditandai dengan makan obsesif, obesiti, keterbelakangan mental, dan alat kelamin kecil.
CORSICA BUKU YANG BERKAIT DENGAN «PRADER-WILLI SYNDROME»
Ketahui penggunaan
Prader-Willi syndrome dalam pilihan bibliografi berikut. Buku yang berkait dengan
Prader-Willi syndrome dan ekstrak ringkas dari yang sama untuk menyediakan konteks penggunaannya dalam kesusasteraan Corsica.
1
Prader-
Willi Syndrome: Development and Manifestations
Both authors have been involved in the Cambridge PWS study, which is the largest and most rounded of the cohort studies of PWS anywhere in the world. The unique data it provides is the basis of this book.
Joyce Whittington, Tony Holland,
2004
2
Management of
Prader-
Willi Syndrome
This manual is endorsed by The Prader-Willi Syndrome Association, which is recognized world-wide.
Merlin Butler, Phillip D.K. Lee, Barbara Y. Whitman,
2006
3
Prader-
Willi Syndrome: A Practical Guide
An examination of the cognitive, medical and psychological aspects of educating a child with Prader-Willi Syndrome.
4
Prader-
Willi Syndrome: Effects of Human Growth Hormone Treatment
This book provides an overview of the clinical research results as to hormones and metabolism of PWS with special emphasis on growth hormone and growth hormone treatment.
5
Prader-
Willi Syndrome: Selected Research and Management Issues
This volume is not intended as a comprehensive review, but as a source of new, original research on this little understood syndrome.
Mary L. Caldwell, Ronald L. Taylor,
2011
6
Management of
Prader-
Willi Syndrome: Under the Sponsorship ...
Management of Prader-Willi Syndrome is the first book to provide a comprehensive source of knowledge about Prader-Willi Syndrome and to offer common-sense guidelines for management.
Louise R. Greenswag, Randell C. Alexander,
2012
7
Prader-
Willi Syndrome: New Insights for the Healthcare ...
Prader-Willi Syndrome: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Prader-Willi Syndrome in a compact format.
8
Hypothalamic Regulation in Relation to Maladaptive, ...
Prader-Willi Syndrome (PWS) is a neurogenetic disorder that occurs in 1 in approximately 20,000 and is the leading cause of genetic obesity.
9
Prader-
Willi Syndrome as a Model for Obesity: International ...
37 Lee PDK: Endocrine and metabolic aspects of Prader-Willi syndrome; in
Greenswag LR, Alexander R (eds): Management of the Prader-Willi Syndrome.
New York, Springer,1995, pp 32–57. 38 Cassidy SB: Prader-Willi syndrome.
Urs Eiholzer, Dagmar l'Allemand,
2003
10
Neurodevelopmental Disorders
Visual processing strengths also are suggested by Gabel et al. (1986), who
administered a battery of attentional, visuospatial, and psychomotor tasks to 15
children with Prader-Willi syndrome and 15 age- and gender-matched normal
children.
Helen Tager-Flusberg,
1999
BARANGAN BERITA YANG TERMASUK TERMA «PRADER-WILLI SYNDROME»
Ketahui apa yang diterbitkan oleh akhbar nasional dan antarabangsa dan cara istilah
Prader-Willi syndrome digunakan dalam konteks perkara berita berikut.
Walk or run to support Prader-Willi Syndrome research
Prader-Willi Syndrome (PWS) is a rare genetic disorder, affecting approximately one in 15,000 births, and causes constant hunger, short stature ... «Pamplin Media Group, Jul 15»
Aeterna Zentaris Commences Promotional Activities for EMD …
... or in children with Prader-Willi syndrome who are severely overweight or have a history of breathing problems including sleep apnea. «MarketWatch, Jul 15»
Special needs woman, toddler, still missing in Gary
Bynum has Prader-Willi syndrome and is said to think at the level of a 5- to 7-year-old. "She takes meds three times a day which helps her focus ... «WLS-TV, Jul 15»
Photographer Rachel Callander's wonderful gift to families of …
... featured in the book all have genetic or chromosomal conditions such as Down syndrome, Angelman syndrome and Prader-Willi syndrome. «Sydney Morning Herald, Jul 15»
Chinese scientists identify new therapy for child obesity
... metabolites, and said an improved gut microbiota can significantly help to treat genetic obesity such as Prader-Willi Syndrome (PWS). «WantChinaTimes, Jul 15»
Zafgen Downgraded by Zacks (ZFGN)
... and hyperphagia in Prader-Willi Syndrome patients, craniopharyngioma-associated obesity, and severe obesity in the general population. «WKRB News, Jul 15»
Cyclists tackle ride for a cause
With the addition of this year's fundraising, Scott estimates that they have donated about $100,000 to the Prader-Willi Syndrome Association ... «Snohomish County Tribune, Jul 15»
Zafgen Lowered to "Hold" at Zacks (ZFGN)
... and hyperphagia in Prader-Willi Syndrome patients, craniopharyngioma-associated obesity, and severe obesity in the general population. «Dakota Financial News, Jul 15»
Study helps kids with obesity gene
BEIJING, July 23 (Xinhuanet) -- A research team has successfully helped children with Prader-Willi Syndrome, a kind of hereditary obesity, lose ... «Xinhua, Jul 15»
JEFF EDELSTEIN: Chris Christie caves on plan to displace 470 …
“It's a full victory,” said Henoch, who has 27-year-old daughter, Sophie, who has Prader-Willi Syndrome and lives at Prader-Willi Homes of ... «The Trentonian, Jul 15»