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Distal trisomy 2p
Distal trisomy 2q
Distal trisomy 3p
Distal trisomy 4q
Distal trisomy 6q
Distal trisomy 7p
Distal trisomy 9q

Translation of "trisomy d syndrome " (English → French) :

TERMINOLOGY
see also In-Context Translations below
A rare chromosomal anomaly syndrome resulting from partial trisomy of the long arm of chromosome 20 with high phenotypic variability. The disease has characteristics of neurodevelopmental delay, cardiac malformations (ventricular septal defect, coarc
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trisomie distale 20q
SNOMEDCT-BE (ventricular septal defect, coarc / 764500002
SNOMEDCT-BE (disorder) / 764500002
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A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c
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leucémie aigüe myéloïde héréditaire
SNOMEDCT-BE (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c / 764940002
SNOMEDCT-BE (disorder) / 764940002
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A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib
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syndrome de Mœbius
SNOMEDCT-BE (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib / 89444000
SNOMEDCT-BE (disorder) / 89444000
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Distal trisomy 7p
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trisomie distale 7p
SNOMEDCT-BE (disorder) / 763276000
SNOMEDCT-BE (disorder) / 763276000
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Distal trisomy 6q
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trisomie distale 6q
SNOMEDCT-BE (disorder) / 763275001
SNOMEDCT-BE (disorder) / 763275001
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Distal trisomy 2q
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trisomie distale 2q
SNOMEDCT-BE (disorder) / 763272003
SNOMEDCT-BE (disorder) / 763272003
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Distal trisomy 2p
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trisomie distale 2p
SNOMEDCT-BE (disorder) / 764518004
SNOMEDCT-BE (disorder) / 764518004
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Distal trisomy 3p
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trisomie distale 3p
SNOMEDCT-BE (disorder) / 764519007
SNOMEDCT-BE (disorder) / 764519007
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Distal trisomy 4q
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trisomie distale 4q
SNOMEDCT-BE (disorder) / 763273008
SNOMEDCT-BE (disorder) / 763273008
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Distal trisomy 9q
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trisomie distale 9q
SNOMEDCT-BE (disorder) / 764520001
SNOMEDCT-BE (disorder) / 764520001
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IN-CONTEXT TRANSLATIONS
The most common type of Down syndrome is trisomy 21, which accounts for 95% of all cases.
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Le type de syndrome de Down le plus fréquent, qui compte pour 95 % des cas, est la trisomie 21.
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http://fr.healthierchoices.ca/ (...) [HTML]
When there are anomalies, the two homologous chromosomes may remain linked to each other, and thus migrate to the same pole and end up in the same gamete (cause of trisomy 21, or Down syndrome, for example).
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En cas d’anomalies, les deux chromosomes homologues peuvent rester liés, migrer vers le même pôle et ainsi se retrouver dans le même gamète (à l’origine de la trisomie 21 par exemple).
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Trisomy 21, also known as Down’s syndrome, affects the child’s intellectual development.
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La trisomie 21, également appelée syndrome de Down, affecte le développement intellectuel de l’enfant.
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http://sante.gouv.qc.ca/consei (...) [HTML]


Others have searched : distal trisomy 2p    distal trisomy 2q    distal trisomy 3p    distal trisomy 4q    distal trisomy 6q    distal trisomy 7p    distal trisomy 9q    trisomy d syndrome    


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'trisomy d syndrome'

Date index:2023-02-27 -

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