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Hypergonadotrophic hypogonadism
Hypogonadism with anosmia
Hypogonadotrophic hypogonadism
Hypogonadotropic hypogenitalism
Hypogonadotropic hypogonadism
Kallmann syndrome
Kallmann's syndrome
Olfactory genital dysplasia
Primary hypogonadism
Secondary hypogenitalism
Secondary hypogonadism

Traduction de «hypogonadism with anosmia » (Anglais → Français) :

Kallmann's syndrome [ hypogonadism with anosmia | Kallmann syndrome | olfactory genital dysplasia ]

dysplasie olfactogénitale [ syndrome de Morsier-Kallmann | dysplasie olfacto-génitale | syndrome de Morsier ]


hypergonadotrophic hypogonadism | primary hypogonadism

hypergonadisme hypergonadotrophique | hypergonadisme primitif


hypogonadotropic hypogenitalism | hypogonadotropic hypogonadism | secondary hypogenitalism | secondary hypogonadism

hypogénitalisme hypogonadotrophique | hypogénitalisme secondaire | hypogonadisme hypogonadotrophique | hypogonadisme secondaire


hypogonadotrophic hypogonadism | secondary hypogonadism

hypogonadisme hypogonadotrophique | hypogonadisme secondaire


A very rare syndrome with characteristics of the association of Mobius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic.

syndrome de Moebius-neuropathie axonale-hypogonadisme hypogonadotrope


5-Alpha-reductase deficiency (with male pseudohermaphroditism) Defective biosynthesis of testicular androgen NOS Testicular hypogonadism NOS

Biosynthèse défectueuse de l'hormone androgène testiculaire SAI Déficit en 5-alpha-réductase (avec pseudo-hermaphroditisme masculin) Hypogonadisme testiculaire SAI


X-linked intellectual deficit Van Esch type has characteristics of mild to moderate intellectual deficit associated with low birth weight, short stature, microcephaly and variable hypergonadotropic hypogonadism. It has been described in seven males f

déficience intellectuelle liée à l'X type Van Esch


An extremely rare neurodegenerative disorder characterized by progressive spinocerebellar ataxia, sensorineural hearing loss, and hypergonadotropic hypogonadism associated with additional neurological manifestations (such as peripheral muscle wasting

syndrome de Richards-Rundle




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Date index: 2024-07-21
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