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EVALUATION OF PLASMA SUBSTANCE P AND BETA‐ENDORPHIN LEVELS IN CHILDREN WITH PRADER‐WILLI SYNDROME
BACKGROUND: Prader-Willi syndrome (PWS) is a rare obesity-related genetic disorder often caused by a deletion of the chromosome 15q11–q13 region inherited from the father or by maternal disomy 15. Growth hormone deficiency with short stature, hypogonadism, cognitive and behavioral problems, analgesi...
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| Publicat a: | J Rare Disord |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4997806/ https://ncbi.nlm.nih.gov/pubmed/27570781 |
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