Waterhouse-Friderichsen syndrome [ meningococcal Waterhouse-Friderichsen syndrome | meningococcal hemorrhagic adrenalitis | meningococcal haemorrhagic adrenalitis | fulminant meningococcal sepsis with adrenal apoplexy | purpura fulminans (Waterhouse-Friderichsen syndrome) ]

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syndrome de Waterhouse-Friderichsen [ surrénalite hémorragique à méningocoques | syndrome méningococcique surrénalien ]

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adrenogenital syndromes, virilizing or feminizing, whether acquired or due to adrenal hyperplasia consequent on inborn enzyme defects in hormone synthesis female:adrenal pseudohermaphroditism | heterosexual precocious pseudopuberty | male:isosexual precocious pseudopuberty | macrogenitosomia praecox | sexual precocity with adrenal hyperplasia | virilization (female)

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macrogénitosomie précoce | précocité sexuelle avec hyperplasie surrénale | pseudo-puberté isosexuelle précoce | chez l'homme | pseudo-hermaphrodisme surrénalien | pseudo-puberté hétérosexuelle précoce | chez la femme | syndromes génito-surrénaliens, masculinisant ou féminisant, qu'ils soient acquis ou associés à une hyperplasie surrénale congénitale consécutive à des anomalies enzymatiques congénitales de la synthèse des hormones cortico-stéroïdes virilisme (chez la femme)

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addisonian crisis [ adrenal crisis | acute adrenocortical insufficiency | Bernard-Sergent syndrome ]

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crise addisonienne [ insuffisance surrénale aiguë | crise corticosurrénalienne | crise surrénalienne ]

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Conn's syndrome Primary aldosteronism due to adrenal hyperplasia (bilateral)

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Hyperaldostéronisme primaire dû à un adénome surrénalien (bilatéral) Syndrome de Conn

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Syndrome with characteristics of various anomalies of the endocrine, cerebral, and skeletal systems resulting in neonatal mortality. Six cases from consanguineous parents have been described. Endocrine anomalies include hypoplasia of the adrenal and

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syndrome endocrino-cérébro-ostéodysplasique

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A very rare form of multiple endocrine neoplasia, an inherited cancer syndrome, with parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors. Caused by heterozygous inactivating mutations in t

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néoplasie endocrinienne multiple type 4

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D'autres ont cherché : bernard-sergent syndrome acute adrenocortical insufficiency addisonian crisis adrenal crisis hepato-adrenal syndrome hepato-nephritic syndrome hepato-ovarian syndrome heterosexual precocious pseudopuberty macrogenitosomia praecox male isosexual precocious pseudopuberty meningococcal haemorrhagic adrenalitis meningococcal hemorrhagic adrenalitis purpura fulminans sexual precocity with adrenal hyperplasia virilization

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'hepato-adrenal syndrome' ->

Date index: 2022-01-06