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Chromosome remplacé par un anneau ou dicentrique
Syndrome de l'X fragile
Syndrome du chromosome 5 en anneau
Syndrome du chromosome 7 en anneau
Syndrome du chromosome X fragile
Syndrome du chromosome Y en anneau

Translation of "Syndrome du chromosome 5 en anneau " (French → English) :

TERMINOLOGY
see also In-Context Translations below
syndrome du chromosome 5 en anneau

A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are a neonatal mewing cry, severe developmental delay and intellectual disability, short stature, hypotonia, dysmorphic features (including microcephaly,
SNOMEDCT-BE (disorder) / 765487008
SNOMEDCT-BE (including microcephaly, / 765487008


syndrome du chromosome 7 en anneau

A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are growth failure, short stature, intellectual disability, dermatological abnormalities (nevus flammeus, dark pigmented nevi, cafe au lait spots), microc
SNOMEDCT-BE (disorder) / 765489006
SNOMEDCT-BE (nevus flammeus, dark pigmented nevi, cafe au lait spots), microc / 765489006


syndrome du chromosome Y en anneau

A rare chromosome Y structural anomaly, with a highly variable phenotype, mostly characterised by short stature, partial to total gonadal failure, sexual infantilism, genital anomalies (e.g. ambiguous genitalia, hypospadias, cryptorchidism), and azoo
SNOMEDCT-BE (disorder) / 763407008
SNOMEDCT-BE (e.g. ambiguous genitalia, hypospadias, cryptorchidism), and azoo / 763407008


syndrome de l'X fragile | syndrome du chromosome X fragile

fragile x chromosome syndrome | fragile X syndrome | Fra-X syndrome | FRAXA syndrome | Martin-Bell syndrome | FRAX [Abbr.] | FXS [Abbr.]
IATE - Health
IATE - Health


Chromosome remplacé par un anneau ou dicentrique

Chromosome replaced with ring or dicentric
WORLD HEALTH ORGANIZATION ICD-10: Q93.2
WORLD HEALTH ORGANIZATION ICD-10: Q93.2


Syndrome de Klinefelter, homme avec plus de deux chromosomes X

Klinefelter's syndrome, male with more than two X chromosomes
WORLD HEALTH ORGANIZATION ICD-10: Q98.1
WORLD HEALTH ORGANIZATION ICD-10: Q98.1
IN-CONTEXT TRANSLATIONS
Quant à la date, elle symbolise ce vingt-et-unième chromosome supplémentaire que possèdent 95 p. 100 des personnes qui souffrent du syndrome de Down.

The date stands as a symbol for the extra twenty-first chromosome that 95 per cent of people with Down syndrome have.


Le syndrome de Down est une anomalie chromosomique congénitale provoquée par la présence d'un chromosome supplémentaire sur la 21paire.

Down syndrome is a naturally occurring arrangement of chromosomes in which extra material is present in the twenty-first chromosome.


Du point de vue scientifique, c'est inacceptable que l'homme ait plus de 40 ou 45 ans pour donner du sperme à cause de la possibilité accrue du syndrome de Down et toutes les autres possibilités de chromosomes anormaux.

Scientifically, it's unacceptable for a man to be over the age of 40 or 45 to be a sperm donor, because of the possibility of an increased risk of Down's syndrome, or any other possible chromosomal anomalies.


À titre d'exemple, il y a un marqueur situé sur le chromosome 21 et trois copies de ce chromosome sont des mutations viables, comme c'est le cas pour le syndrome de Down.

For example, there happens to be a marker on chromosome 21 and three copies of that chromosome are compatible with life — we see that in Down syndrome.


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Ce type de profilage permet de déceler des anomalies comme une différence dans le nombre de chromosomes sexuels ainsi que le syndrome de Down, que l'on connaît également sous le nom de trisomie 21.

The list of conditions that this type of profiling can detect includes, but is not limited to, any difference in the number of sex chromosomes as well as Down syndrome or what is commonly known as trisomy 21.




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Syndrome du chromosome 5 en anneau

Date index:2023-05-08 -

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