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- W2035525314 endingPage "20" @default.
- W2035525314 startingPage "1" @default.
- W2035525314 abstract "Prader–Willi syndrome (PWS) is a neurodevelopmental disorder that arises from lack of expression of paternally inherited genes known to be imprinted and located in the chromosome 15q11-q13 region. PWS is considered the most common syndromal cause of life-threatening obesity and is estimated at 1 in 10 000 to 20 000 individuals. A de novo paternally derived chromosome 15q11-q13 deletion is the cause of PWS in about 70% of cases, and maternal disomy 15 accounts for about 25% of cases. The remaining cases of PWS result either from genomic imprinting defects (microdeletions or epimutations) of the imprinting centre in the 15q11-q13 region or from chromosome 15 translocations. Here, we describe the clinical presentation of PWS, review the current understanding of causative cytogenetic and molecular genetic mechanisms, and discuss future directions for research." @default.
- W2035525314 created "2016-06-24" @default.
- W2035525314 creator A5045905377 @default.
- W2035525314 creator A5065335322 @default.
- W2035525314 date "2005-07-25" @default.
- W2035525314 modified "2023-10-03" @default.
- W2035525314 title "Prader–Willi syndrome: clinical genetics, cytogenetics and molecular biology" @default.
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