Macroscopical syndromes

Articles

• fibrinous inflammation
  17 October 2005

  In severe injuries resulting in great vascular permeability, larger molecules such as fibrinogen pass the vascular barrier, and fibrin is formed and deposited in the extracellular space.
  A fibrinous exudate develops when the vascular leaks are large enough or there is a procoagulant stimulus in the interstitium (e.g., cancer cells).
  A fibrinous exudate is characteristic of inflammation in the lining of body cavities, such as the meninges (fibrinous meningitis), pericardium (fibrinous (...)

• caudal dysplasia
  5 April 2004

  caudal dysplasia syndrome, caudal regression, caudal dysplasia, sacral agenesis syndrome, caudal dysgenesis, caudal regression syndrome, caudal dysgenesis defect

• non-dysplastic renal hypoplasia
  23 May 2007

  NDRH, nondysplastic renal hypoplasia

• non-syndromic BNOMRD
  21 March 2007

  non-syndromic bilateral non-obstructive multicystic renal dysplasia, non-syndromal BNORD, nonsyndromal diffuse cystic renal dysplasia, non-syndromal DCRD, non-syndromal DRD, non-syndromal diffuse renal dysplasia, non-syndromic bilateral non-obstructive renal dysplasia, isolated bilateral non-obstructive multicystic renal dysplasia (MRD).

• XX DSD
  18 May 2005

  XX intersex; XX disorders of sexual development

• hydronephrosis
  25 August 2005

  See also
  fetal hydronephrosis

• Cystic kidneys
  25 May 2005

  Types
  monocystic kydneys
  oligocystic kidneys
  multicystic kidneys (polycystic kidneys) polycystic kidney diseases (PKDs) autosomal recessive polycystic kidney diseases (ARPKDs) autosomal dominant kidney diseases (ADPKDs) other polycystic kidney diseases (OPKDs) multicystic renal dysplasia
  References
  Bisceglia M, Galliani CA, Senger C, Stallone C, Sessa A. Renal cystic diseases: a review. Adv Anat Pathol. 2006 Jan;13(1):26-56. PMID: #16462154#
  Hildebrandt F, Otto E. Cilia and (...)

• varioliform gastritis
  21 January 2004
• metabolic cirrhosis
  25 October 2005

  Types
  hereditary tyrosinemia
  galactosemia
  Wolman disease
  cerebrohepatorenal syndrome (Zellweger syndrome)
  glycogen storage disease type IV (GSD4)
  indian childhood cirhosis
  alpha-antitrypsin deficiency
  Wilson disease
  mitochondrial respiratory chain diseases
  neonatal adrenoleukodystrophy
  infantile Refsum disease
  familial cholestatic syndromes
  mucopolysaccharidoses
  sialidosis
  Gaucher disease
  Niemann-Pick diseases (...)

• bilateral multicystic kidneys
  3 December 2004

  bilateral diffuse multicystic kidneys

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