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PCOS
Polycystic ovarian syndrome
Polycystic ovary syndrome
Resistant ovary syndrome
Sclerocystic ovary syndrome Stein-Leventhal syndrome
Stein-Leventhal syndrome

Translation of "polycystic ovary syndrome " (English → French) :

polycystic ovary syndrome | PCOS | polycystic ovarian syndrome | Stein-Leventhal syndrome

syndrome des ovaires polykystiques | SOPK | syndrome de Stein-Leventhal
médecine > sémiologie et pathologie | médecine > gynécologie et obstétrique
médecine > sémiologie et pathologie | médecine > gynécologie et obstétrique


polycystic ovary syndrome | polycystic ovarian syndrome [Abbr.]

SOPK | syndrome des ovaires polykystiques
IATE - Health
IATE - Health


Stein-Leventhal syndrome [ polycystic ovary syndrome ]

syndrome de Stein-Leventhal [ syndrome des ovaires polykystiques ]
Genitourinary Tract
Appareil génito-urinaire


resistant ovary syndrome

syndrome d'ovaires résistants
The Genitals
Organes génitaux


Polycystic ovarian syndrome

Syndrome ovarien polykystique
WORLD HEALTH ORGANIZATION ICD-10: E28.2
WORLD HEALTH ORGANIZATION ICD-10: E28.2


Sclerocystic ovary syndrome Stein-Leventhal syndrome

Syndrome (de):ovarien sclérokystique | Stein-Leventhal
WORLD HEALTH ORGANIZATION ICD-10: E28.2
WORLD HEALTH ORGANIZATION ICD-10: E28.2


Decreased estrogen Premature menopause NOS Resistant ovary syndrome

Diminution des œstrogènes Ménopause prématurée SAI Syndrome de l'ovaire résistant aux gonadotrophines
WORLD HEALTH ORGANIZATION ICD-10: E28.3
WORLD HEALTH ORGANIZATION ICD-10: E28.3


Tuberous sclerosis, polycystic kidney disease contiguous gene syndrome

polykystose rénale autosomique dominante type 1 avec sclérose tubéreuse
SNOMEDCT-BE (disorder) / 765331004
SNOMEDCT-BE (disorder) / 765331004


A rare developmental defect during embryogenesis syndrome, with characteristics of normal female karyotype, normal ovaries, male or ambiguous genitalia, urinary tract malformations (ranging from bilateral renal agenesis to mild unilateral hydronephro

syndrome d'anomalie du développement sexuel 46,XX-anomalies anorectales
SNOMEDCT-BE (ranging from bilateral renal agenesis to mild unilateral hydronephro / 733622000
SNOMEDCT-BE (disorder) / 733622000


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

syndrome d'hypogonadisme hypergonadotrope primaire-alopécie partielle
SNOMEDCT-BE (disorder) / 719275009
SNOMEDCT-BE (disorder) / 719275009




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'polycystic ovary syndrome'

Date index:2023-07-08 -

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