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Significados de complete trisomy 21 syndrome em inglês

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даунизм
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mongolismo
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mongolismo
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trisomia 21
Wikidata

Chromosomal condition characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability.

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      My younger brother, who is now 18, suffers from Downs Syndrome.
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      1
      Conclusions: Mothers' knowledge about the screening tests for trisomy 21 remains fragmentary.
      Pubmed
      2
      Objective: To assess mothers' knowledge of screening tests for trisomy 21.
      Pubmed
      3
      Such a finding would normally suggest a postzygotic origin of the trisomy 21.
      Pubmed
      4
      Conclusions: FISH-based scanning can identify trisomy 21 pregnancies by analysis of routine cervical brushings.
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      5
      This study provides new evidence regarding an important source of reactive oxygen species in trisomy 21.
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