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Alopécie
Alopécie androgénogénetique
Alopécie cicatricielle
Chute
Partielle ou générale) des poils ou des cheveux
Solution d'alopécie

Translation of "Solution d'alopécie " (French → English) :

solution d'alopécie

Alopecia solution
SNOMEDCT-BE (physical object) / 701781007
SNOMEDCT-BE (physical object) / 701781007


alopécie | chute (temporaire | partielle ou générale) des poils ou des cheveux

alopecia | baldness
UGENT - Medical terms -
UGENT - Medical terms -


alopécie androgénogénetique

Common baldness
SNOMEDCT-BE (disorder) / 87872006
SNOMEDCT-BE (disorder) / 87872006




syndrome d'alopécie-contractures-nanisme-déficience intellectuelle

A form of ectodermal dysplasia syndrome with characteristics of short stature of prenatal onset, alopecia, ichthyosis, photophobia, ectrodactyly, seizures, scoliosis, multiple contractures, fusions of various bones, particularly elbows, carpals, meta
SNOMEDCT-BE (disorder) / 720979002
SNOMEDCT-BE (disorder) / 720979002


kératodermie palmoplantaire et alopécie congénitale autosomique dominante

Palmoplantar keratoderma and congenital alopecia Stevanovic type
SNOMEDCT-BE (disorder) / 719518004
SNOMEDCT-BE (disorder) / 719518004


alopécie cicatricielle

Alopecia cicatrisata
SNOMEDCT-CA (trouble) / 400088006
SNOMEDCT-CA (trouble) / 400088006


syndrome d'alopécie-déficience intellectuelle-hypogonadisme hypergonadotrope

This syndrome has characteristics of the association of total alopecia (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism. It has been described in two brothers born to non consanguineous parents of Caucasian origin. Ele
SNOMEDCT-BE (disorder) / 720981000
SNOMEDCT-BE (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism. It has been described in two brothers born to non consanguineous parents of Caucasian origin. Ele / 720981000


syndrome d'hypogonadisme hypergonadotrope-alopécie fronto-pariétale

Salti Salem syndrome
SNOMEDCT-BE (disorder) / 721842008
SNOMEDCT-BE (disorder) / 721842008


syndrome d'hypogonadisme hypergonadotrope primaire-alopécie partielle

This syndrome is characterized by primary hypergonadotropic hypogonadism and partial alopecia. So far, it has been described in seven patients from three families. Mullerian hypoplasia, absent or streak ovaries, hypoplastic internal genitalia and pri
SNOMEDCT-BE (disorder) / 719275009
SNOMEDCT-BE (disorder) / 719275009




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Solution d'alopécie

Date index:2022-09-03 -

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