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  • Prader-Willi syndrome
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  • prader-willi syndrome
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PLWS Prader-Labhart-Willi syndrome
PWCR Prader-Willi chromosome region
PWS port wine stain; Prader-Willi syndrome
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PWS Prader Willi
PWS Prader Willi syndrome
PLWS Prader-Labhard-Willi Syndrome
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  • Prader-Willi syndrome
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Prader, Andrea <person> Swiss paediatrician, *1919.
See: Prader-Willi syndrome.
(05 Mar 2000)
prader-willi syndrome <syndrome> A condition in children with floppiness (hypotonia), obesity, small hands and feet and mental retardation. It is due to loss of part or all of chromosome 15, specifcally the chromosome 15 from the father. The fat and red-faced boy in a state of somnolency described by charles dickens in his novel the pickwick papers is thought by some to have had prader-willi syndrome. (the same boy inspired the naming of the pickwickian syndrome).
(12 Dec 1998)
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syndrome, prader-willi A condition in children with floppiness (hypotonia), obesity, small hands and feet and mental retardation. It is due to loss of part or all of chromosome 15, specifcally the chromosome 15 from the father. The fat and red-faced boy in a state of somnolency described by charles dickens in his novel the pickwick papers is thought by some to have had prader-willi syndrome. (the same boy inspired the naming of the pickwickian syndrome).
(12 Dec 1998)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Prader-Willi Syndrome - »õâ An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 from the mother (UNIPARENTAL DISOMY) which are imprinted (GENETIC IMPRINTING) and hence silenced. Clinical manifestations include MENTAL RETARDATION; MUSCULAR HYPOTONIA; HYPERPHAGIA; OBESITY; short stature; HYPOGONADISM; STRABISMUS; and HYPERSOMNOLENCE. (Menkes, Textbook of Child Neurology, 5th ed, p229)
    Synonyms : Labhart-Willi-Prader-Fanconi Syndrome, Royer's Syndrome, Labhart Willi Prader Fanconi Syndrome, Labhart Willi Syndrome, Prader Willi Syndrome, Royers Syndrome, Syndrome, Labhart-Willi, Syndrome, Labhart-Willi-Prader-Fanconi, Syndrome, Prader-Willi
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Prader-Willi syndrome a genetic disorder of chromosome 15 marked by hypotonia, short stature, hyperphagia, cognitive impairment, poor feeding and growth in infancy, and when not carefully managed, characterized by obesity
Ãâó: depts.washington.edu/pwdlearn/web/glossary/glossar...
Prader-Willi syndrome A combination of birth defects caused by inheriting both copies of a section on the #15 chromosome from the mother or by inheriting a deletion of a region of chromosome #15 from the father.
Ãâó: www.uchicagokidshospital.org/online-library/conten...
Prader-Willi syndrome a condition characterized by obesity and insatiable appetite, mental deficiency, small genitalia, and short stature. May be caused by a deletion on chromosome 15 or maternal UPD15. More on Prader-Willi syndrome...
Ãâó: www.medgen.ubc.ca/wrobinson/mosaic/glossary.htm
Prader o. a string of plastic models of testes, marked according to their volume in cubic centimeters; used for measuring the size of the testes either in growing boys or in men who have an abnormal condition or have had a procedure done.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
Prader-Willi s. a congenital disorder characterized by obesity, short stature, lack of muscle tone, hypogonadism, and central nervous system dysfunction; there is often a characteristic rounded face with almond-shaped eyes and a low forehead. Mental retardation is common. It can be caused by a deletion on chromosome 15 inherited from the father; the same deletion inherited from the mother causes Angelman's syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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