Prader-Willi syndrome: an update on obesity and endocrine problems
Prader-Willi syndrome (PWS) is a rare complex genetic disorder that results from a lack of expression of the paternally inherited chromosome 15q11-q13. PWS is characterized by hypotonia and feeding difficulty in early infancy and development of morbid obesity aggravated by uncontrolled hyperphagia a...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Korean Society of Pediatric Endocrinology,
2021-12-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |