Although Prader-Willi syndrome is a rare disease, it provides an excellent example of how early diagnosis and meticulous management can significantly improve long-term prognosis of some genetic diseases. These guidelines, particularly addressed to family paediatricians, provide a brief and practical summary on how to diagnose and to manage the different physical and behavioural problems of patients with Prader-Willi syndrome.
|Number of pages||1|
|Journal||Medico e Bambino|
|Publication status||Published - Mar 2012|
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health