Morbus Addisonianus

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Morbus Addisonianus est morbus endocrineus rarus, quo glandularum suprarenalium functio diminuta (insufficientia glandualrum suprarenalium) est. Hac de causa synthesis hormontis cortisoli reducta est. Saepissime morbus Addisonianus morbus autoimmunitatis imponit[1]. In infantibus vero geneticae causae morbum Addisonianum adclarant[2].

Symptomata sunt fatigatio, musculorum imbecilitas, abdominis dolor. Periculosissima est crisis Addisoniana, imprimis in aliorum morborum vel contagionis coniunctione[3].

Tractatio hormontum supplementum includit[4], imprimis circum operationes chirurgicas et graviores animi contentiones.

  1. Hellesen A., Bratland E., Husebye E. S. (Iun 2018). "Autoimmune Addison's disease - An update on pathogenesis". Annales d'endocrinologie 79 (3): 157-63 
  2. Betterle C., Presotto F., Furmaniak J. (Dec 2019). "Epidemiology, pathogenesis, and diagnosis of Addison's disease in adults". Journal of endocrinological investigation 42 (12): 1407-33 
  3. Smans L. C. C. J., Van der Valk E. S., et al. (Ian 2016). "Incidence of adrenal crisis in patients with adrenal insufficiency". Clinical endocrinology 84 (1): 17-22 
  4. Napier C., Pearce S. H. S. (Iun 2014). "Current and emerging therapies for Addison's disease". Current opinion in endocrinology, diabetes, and obesity 21 (3): 147-53 

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