Disease group (etiology)

Articles

• hereditary hyperfunctions of endocrine cells
  19 June 2004

  hereditary hyperfunction disorders of endocrine cells

• WT1-associated diseases
  11 May 2004

  WT1 mutations-associated disorders, WT1-related diseases, WT1-related disorders

• arboviroses
  6 February 2006

  Exemples
  yeloow fever
  dengue
  chikungunya
  Kyasanur Forest disease
  PAthogeny
  Etiologic agents of arboviral diseases are primarily zoonotic pathogens that are maintained in nature in cycles involving arthropod transmission among a variety of susceptible reservoir hosts.
  In the simplest form of human exposure, spillover occurs from the enzootic cycle when humans enter zoonotic foci and/or enzootic amplification increases circulation near humans.
  Examples include Eastern equine (...)

• echinococcosis
  5 December 2005

  hydatid disease
  Definition: Echinococcosis, which is often referred to as hydatid disease or echinococcal disease, is a parasitic disease that affects both humans and other mammals, such as sheep, dogs, rodents and horses.
  Images
  hepatic cystic echinococcosis / Echinococcus granulosus
  https://twitter.com/RhondaYantiss/status/851519941299851265
  There are three different forms of echinococcosis found in humans, each of which is caused by the larval stages of different species of the (...)

• inborm errors of thyroid metabolism
  21 November 2005

  Types
  TSH unresponsiveness
  iodine tranposrt defect
  organification defect
  coupling defect
  anomalies of thyroglobulin synthesis and secretion
  deiodinase defect
  anomalies of thyroid hormone transport
  other defects
  See also
  Thyroid

• defective iodide transport diseases
  23 November 2005

  Synopsis
  large congenital goiter (up to 150 g).
  hypothyroidism
  atypical cells
  hyperplastic pattern with predominant microfollicular aspect
  Electron microscopy
  hyperactive follicular cell with folding of the basal membrane
  See also
  NIS symporter protein mutations
  References
  Camargo RY, Gross JL, Silveiro SP, Knobel M, Medeiros-Neto G. Pathological Findings in Dyshormonogenetic Goiter with Defective Iodide Transport. Endocr Pathol. 1998 Autumn;9(3):225-233. PMID: (...)

• thyroid metabolism diseases
  23 November 2005

  inherited disorders of thyroid metabolism, inborn errors of thyroid metabolism

• cerebral vascular diseases
  11 November 2004

  Exemples
  cerebral hemorrhage

• hepatic storage diseases
  15 June 2004

  Digital cases
  Case 247 : glycogen storage disease type 3 - GSD3
  Types
  mucopolysaccharidoses
  mannosidosis/fucosidosis
  sialidosis
  mucolipidosis
  GM1 general gangliosidosis
  cystinosis
  metachromatic leukodystrophy
  Farber disease
  glycogen storage diseases glycogen storage disease type 1 (GSD1) glycogen storage disease type 2 (GSD2) glycogen storage disease type 3 (GSD3) glycogen storage disease type 4 (GSD4)
  hepatic lysosomal storage diseases Wolman disease Gaucher (...)

• multiple endocrine neoplasia syndromes
  19 May 2004

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