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Adiposo-genital syndrome
Adrenogenital syndrome
Apert's hirsutism
Apert-Gallais syndrome
Cooke-Apert-Gallais syndrome
Genital dwarfism
Gonodal agenesis
Gonodal aplasis
Hypogonadism with anosmia
Kallmann syndrome
Kallmann's syndrome
Morgagni-Turner syndrome
Morgani-Turner-Albright syndrome
Olfactory genital dysplasia
Ovarian dwarfism
Ovarian short stature syndrome
Primary ovarian insufficiency
Pseudonuchal infantilism
Shereshevskii-Turner syndrome
Suprarenal genital syndrome
Turner's syndrome
Turner-Albright syndrome

Traduction de «Suprarenal genital syndrome » (Anglais → Français) :

adrenogenital syndrome | suprarenal genital syndrome | Apert-Gallais syndrome | Cooke-Apert-Gallais syndrome | Apert's hirsutism

syndrome génitosurrénal | syndrome génito-surrénal | syndrome surrénalogénital | syndrome surrénalo-génital | syndrome surrénogénital | syndrome surréno-génital | syndrome adrénogénital | syndrome adréno-génital | syndrome d'Apert et Gallais | syndrome d'Apert-Gallais | syndrome de Cooke-Apert-Gallais | syndrome de Gallais | hypercorticisme androgénique | hyperandrogénisme surrénalien | syndrome génito-surrénalien | pseudo-hermaphrodisme surrénal | pseudo-hermaphrodisme d'Apert et Gallais


adiposo-genital syndrome

dystrophie adiposo-génitale [ syndrome de Babinski-Froelich ]


Turner's syndrome | Morgagni-Turner syndrome | Morgani-Turner-Albright syndrome | Shereshevskii-Turner syndrome | Turner-Albright syndrome | genital dwarfism | gonodal agenesis | gonodal aplasis | ovarian dwarfism | ovarian short stature syndrome | primary ovarian insufficiency | pseudonuchal infantilism

syndrome de Turner-Albright | agénésie ovarienne | aplasie ovarienne | dysgénésie gonadique | insuffisance gonadique primaire | nanisme ovarien | syndrome de Morgani-Turner-Albright | syndrome de Turner-Varny | syndrome de Ulrich-Turner


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

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


The association of X-linked Alport syndrome with leiomyomatosis of the oesophagus, tracheobronchial tree or female genitals has been reported in more than 30 families. The disease is due to a deletion involving the 5' terminal region of both COL4A5 a

syndrome d'Alport lié à l'X-léiomyomatose diffuse


A multiple malformation syndrome with characteristics of congenital diaphragmatic abnormalities, genital defects and cardiac malformations. Less than 15 patients have been reported worldwide. Ambiguous or female external genitalia are present in indi

syndrome de Meacham-Winn-Culler


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