| 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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