Prader–Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review
Prader–Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review
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Publisher
Switzerland: MDPI AG
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Language
English
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Publisher
Switzerland: MDPI AG
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Scope and Contents
Contents
Prader–Willi syndrome (PWS) is a complex genetic disorder with three PWS molecular genetic classes and presents as severe hypotonia, failure to thrive, hypogonadism/hypogenitalism and developmental delay during infancy. Hyperphagia, obesity, learning and behavioral problems, short stature with growth and other hormone deficiencies are identified du...
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Full title
Prader–Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10002205
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10002205
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ISSN
1422-0067,1661-6596
E-ISSN
1422-0067
DOI
10.3390/ijms24054271
