Article
Hair cortisol-a method to detect chronic cortisol levels in patients with Prader-Willi syndrome
2020-10-29
Abstract excerpt
<title>Abstract</title> <p><bold>Background:</bold> 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 knowledge on long-term cortisol concentrations is lacking. The aim of this st...
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Identifiers and source
- Literature Corpus work
- 2df99476-1aaf-5f6c-889d-f753dadc2e22
- DOI
- 10.21203/rs.3.rs-31626/v5
