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Tegesé saka "Prader-Willi syndrome" ing bausastra Basa Inggris

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ETIMOLOGI SAKA TEMBUNG PRADER-WILLI SYNDROME

After Andrea Prader (1919–2001) and Heinrich Willi (1900–71), Swiss paediatricians.
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Etymology pasinaon babagan asliné tembung lan owahané ing wangun lan teges.
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PANGOCAP SAKA PRADER-WILLI SYNDROME ING BASA INGGRIS

Prader-Willi syndrome  [ˌprɑːdəˈvɪlɪ] play
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GOLONGAN PARAMASASTRA SAKA PRADER-WILLI SYNDROME

tembung aran
tembung sipat
tembung kriya
tembung katrangan
tembung ganti
preposition
panyambung
panemtu
seru

APA TEGESÉ PRADER-WILLI SYNDROME ING BASA INGGRIS?

Klik kanggo deleng deifinisi asli saka «Prader-Willi syndrome» ing bausastra Basa Inggris.
Klik kanggo deleng pertalan otomatis saka definisi ing Basa Jawa.
Prader-Willi syndrome

Sindrom Prader-Willi

Prader–Willi syndrome

Sindrom Prader-Willi (disingkat PWS) yaiku kelainan genetik langka kang pitung gene (utawa sawetara sub bab kasebut) ing kromosom 15 (q 11-13) bakal dibusak utawa ora diterangake (kromosom 15q parsial pambusakan) ing paternal kromosom. Iki pisanan diterangake ing taun 1956 dening Andrea Prader (1919-2001), Heinrich Willi (1900-1971), Alexis Labhart (1916-1994), Andrew Ziegler, lan Guido Fanconi saka Swiss. Karakteristik PWS yaiku "nada otot sing kurang, bangkekan pendek, perkembangan seksual mboten pepak, ora nduweni kognitif, tindak tanduk masalah, lan perasaan kelaparan sing bisa nyebabake obesitas sing ngancam lan ngancam." Insidensi PWS antara 1 saka 25.000 lan 1 saka 10 kelahiran urip. Asal saka materi genetis sing kena pengaruh ing sindrom iki penting amarga wilayah 15 kromosom sing ditandhani tundhuk karo indhustri indhuk asal, tegese manawa kanggo sawetara gen ing wilayah iki mung siji salinan gen kasebut ditulis nalika sing liyane dipungkiri liwat imprinting. Prader–Willi syndrome (/ˈprɑːdər ˈvɪli/; abbreviated P.W.S) is a rare genetic disorder in which seven genes (or some subset thereof) on chromosome 15 (q 11–13) are deleted or unexpressed (chromosome 15q partial deletion) on the paternal chromosome. It was first described in 1956 by Andrea Prader (1919–2001), Heinrich Willi (1900–1971), Alexis Labhart (1916–1994)), Andrew Ziegler, and Guido Fanconi of Switzerland. Characteristic of PWS is "low muscle tone, short stature, incomplete sexual development, cognitive disabilities, problem behaviors, and a chronic feeling of hunger that can lead to excessive eating and life-threatening obesity." The incidence of PWS is between 1 in 25,000 and 1 in 10,000 live births. The maternal origin of the genetic material that is affected in the syndrome is important because the particular region of chromosome 15 involved is subject to parent of origin imprinting, meaning that for a number of genes in this region only one copy of the gene is expressed while the other is silenced through imprinting.

Definisi saka Prader-Willi syndrome ing bausastra Basa Inggris

Definisi sindrom Prader-Willi ing kamus iku kondhisi kongenital sing ditondoi dening obsesif sing obsesif, obesitas, retardasi mental, lan alat kelamin cilik.

The definition of Prader-Willi syndrome in the dictionary is a congenital condition characterized by obsessive eating, obesity, mental retardation, and small genitalia.

Klik kanggo deleng deifinisi asli saka «Prader-Willi syndrome» ing bausastra Basa Inggris.
Klik kanggo deleng pertalan otomatis saka definisi ing Basa Jawa.

TEMBUNG BASA INGGRIS KANG KALARAS PADHA KARO PRADER-WILLI SYNDROME


bailey
ˈbeɪlɪ
billy
ˈbɪlɪ
chile
ˈtʃɪlɪ
chili
ˈtʃɪlɪ
daily
ˈdeɪlɪ
easily
ˈiːzɪlɪ
evilly
ˈiːvɪlɪ
family
ˈfæmɪlɪ
heavily
ˈhevɪlɪ
highly
ˈhaɪlɪ
lily
ˈlɪlɪ
necessarily
ˈnɛsɪsərɪlɪ
nervily
ˈnɜːvɪlɪ
privily
ˈprɪvɪlɪ
savvily
ˈsævɪlɪ
scurvily
ˈskɜːvɪlɪ
top-heavily
ˌtɒpˈhevɪlɪ
uncivilly
ʌnˈsɪvɪlɪ
wavily
ˈweɪvɪlɪ
weevily
ˈwiːvɪlɪ

TEMBUNG BASA INGGRIS KANG AWIT KAYA PRADER-WILLI SYNDROME

Pradesh
Prado
praecipe
praecocial
praecordial
praedial
praediality
praefect
praefectorial
praeludium
praemunire
praenomen
praenomina
praenominal
praenominally
praepostor
Praesepe

TEMBUNG BASA INGGRIS KANG WUSANANÉ KAYA PRADER-WILLI SYNDROME

acute respiratory distress syndrome
aerodrome
airdrome
Asperger´s syndrome
carpal tunnel syndrome
chrome
chronic fatigue syndrome
cosmodrome
fragile-X syndrome
Gilles de la Tourette syndrome
hippodrome
irritable bowel syndrome
Marfan syndrome
metabolic syndrome
sudden infant death syndrome
syndrome
Tourette syndrome
Tourette´s syndrome
toxic shock syndrome
velodrome
Williams syndrome

Dasanama lan kosok bali saka Prader-Willi syndrome ing bausastra dasanama Basa Inggris

DASANAMA

Pertalan saka «Prader-Willi syndrome» menyang 25 basa

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PERTALAN SAKA PRADER-WILLI SYNDROME

Weruhi pertalan saka Prader-Willi syndrome menyang 25 basa nganggo Basa Inggris pamertal multi basa kita.
pertalan saka Prader-Willi syndrome saka Basa Inggris menyang basa liyané kang kasuguhaké ing perangan iki kajupuk saka pertalan statistik otomatis; ing ngendhi inti unit pertalan yaiku tembung «Prader-Willi syndrome» ing Basa Inggris.

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El síndrome de Prader - Willi
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Prader-Willi syndrome
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Síndrome de Prader -Willi
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প্রদার-উইলি সিন্ড্রোম
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Le syndrome de Prader -Willi
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Sindrom Prader-Willi
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Prader -Willi-Syndrom
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프라 더 - 윌리 증후군
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பிராடர்-வில்லி நோய்க்குறி
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प्राडर-विल सिंड्रोम
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Синдром Прадера - Віллі
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Pamertal Basa Inggris - Basa Yunani

Το σύνδρομο Prader - Willi
15 yuta pamicara
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Pamertal Basa Inggris - Basa Afrikaans

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14 yuta pamicara
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Pamertal Basa Inggris - Basa Swedia

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10 yuta pamicara
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Pamertal Basa Inggris - Basa Norwegia

Prader -Willis syndrom
5 yuta pamicara

Trèn migunakaké Prader-Willi syndrome

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KEKAREPAN PANGGUNAN ARAN «PRADER-WILLI SYNDROME»

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Kart kang kapituduh ing dhuwur nuduhaké arang kerepé kagunané aran «Prader-Willi syndrome» ing negara kang béda-béda.
Dhasar kekarepan panggolékan lan kagunaan kang umum saka Prader-Willi syndrome
Daptar dhasar panggolékan kang dilakoni dening pangguna kanggo migunakaké Basa Inggris bausastra online kita lan gupita kang asring digunakaké nganggo tembung «Prader-Willi syndrome».

ARANG KEREPÉ PANGGUNANÉ ARAN «PRADER-WILLI SYNDROME» SALAWASÉ IKI

Gambar awujudaké arang kerepé evolusi taunan panggunané saka tembung «Prader-Willi syndrome» sasuwiné 500 taun. Panggunané andedhasar panalitén sapira asringé aran «Prader-Willi syndrome» metu ing sumber kang kacé digital ing Basa Inggris antaraning taun 1500-an lan wektu iki.

Tuladha kang kagunakaké ing sastra Basa Inggris, pethikan lan warta babaganPrader-Willi syndrome

TULADHA

BUKU BASA INGGRIS KAKAIT KARO «PRADER-WILLI SYNDROME»

Temukaké kagunané saka Prader-Willi syndrome ing pilihan bibliografi iki. Buku kang kakait dening Prader-Willi syndrome lan pethikan cekak kang padha kanggo nyediyakaké panggunané ing sastra Basa Inggris.
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.
Jackie Waters, 1999
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.
Urs Eiholzer, 2001
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.
‎2012
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.
Mayim Chaya Bialik, 2007
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

BABAGAN WARTA KANG NGLEBOKAKÉ ARAN «PRADER-WILLI SYNDROME»

Weruhi yèn pawarta nasional lan internasional wis ngomongaké lan kepriyé aran Prader-Willi syndrome digunakaké ing babagan warta iki.
1
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»
2
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»
3
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»
4
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»
5
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»
6
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»
7
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»
8
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»
9
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»
10
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»

KAITAN
« EDUCALINGO. Prader-Willi syndrome [online]. Kasedya <https://educalingo.com/jv/dic-en/prader-willi-syndrome>. Mei 2024 ».
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