Prader-Willi Syndrome. About a Case
Prader-Willi syndrome is a rare genetic disease, characterized by hypothalamic-pituitary anomalies, which presents with severe hypotonia during the neonatal period and the first two years of life, with hyperphagia with a high risk of developing morbid obesity in childhood and adulthood; as well as l...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Espanhol |
| Publicat: |
Universidad de las Ciencias Médicas de Cienfuegos
2021-04-01
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| Col·lecció: | Revista Finlay |
| Matèries: | |
| Accés en línia: | http://www.revfinlay.sld.cu/index.php/finlay/article/view/869 |
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