Prader-Willi syndrome (Q46700): Difference between revisions
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Síndrome de Prader-Willi é uma doença genética rara caracterizada por anormalidades hipotalâmico-hipofisárias com severa hipotonia durante o período neonatal e nos primeiros dois anos de vida e o aparecimento de hiperfagia com risco de obesidade mórbida durante a infância e a idade adulta, dificuldade de aprendizagem e problemas de comportamento ou problemas psiquiátricos graves. | |||
| description / en | description / en | ||
Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behavioural problems or severe psychiatric problems. | |||
Revision as of 15:28, 13 August 2026
Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behavioural problems or severe psychiatric problems.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD90.3 |
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| English | Prader-Willi syndrome |
Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behavioural problems or severe psychiatric problems. |
