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.
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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.
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LD90.3
    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.

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