| PLWS | Prader-Labhart-Willi syndrome |
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| PWCR | Prader-Willi chromosome region |
| PWS | port wine stain; Prader-Willi syndrome |
| PWS | Prader Willi |
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| PWS | Prader Willi syndrome |
| PLWS | Prader-Labhard-Willi Syndrome |
| Prader, Andrea | <person> Swiss paediatrician, *1919. See: Prader-Willi syndrome. (05 Mar 2000) |
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| 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) |
| 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) |
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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
| 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...
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| 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...
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| 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
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| 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...
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| 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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