Article

The Italian registry for patients with Prader-Willi syndrome

2022-12-08

Abstract excerpt

<title>Abstract</title> <p>Background Prader-Willi syndrome (PWS) is a rare and complex genetic disease, with numerous implications on metabolic, endocrine, neuropsychomotor systems, and with behavioural and intellectual disorders. Rare disease patient registries are important scientific tools i) to collect clinical and epidemiologic data, ii) to assess the clinical management including the diagnostic delay, iii...

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Literature Corpus work: 93d03e09-3fae-5c58-8edd-c9963f34db77
DOI: 10.21203/rs.3.rs-2048478/v1

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