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Hair cortisol-a method to detect chronic cortisol levels in patients with Prader-Willi syndrome
BACKGROUND: Prader-Willi syndrome (PWS) is a multisymptomatic, rare, genetic, neurodevelopmental disorder in adults mainly characterized by hyperphagia, cognitive dysfunction, behavioral problems and risk of morbid obesity. Although endocrine insufficiencies are common, hypocortisolism is rare and k...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | BMC Endocr Disord |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2020
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7654170/ https://ncbi.nlm.nih.gov/pubmed/33167936 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12902-020-00646-w |
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