Clinical syndromes

Articles

• neonatal cholestasis
  3 May 2005

  Types
  neonatal extra-hepatic cholestasis
  neonatal extra-hepatic cholestasis
  ductopenias
  neonatal lobular cholestasis
  Etiology
  neonatal biliary duct diseases
  neonatal extra-hepatic biliary atresia
  neonatal biliary duct paucity (ductopenia)
  neonatal Alagille disease
  Aagenaes syndrome (norwegian)
  north american indian cirrhosis (north american indian cholestasis)
  Greenland eskimo cholestasis
  neonatal intrahepatic cholestasis
  congenital bile acide synthesis defects (...)

• sudden death
  1 July 2003

  Classification:
  sudden cardiac death
  References
  Maron BJ. Sudden death in young athletes. N Engl J Med. 2003 Sep 11;349(11):1064-75. PMID: #12968091#

• hyperparathyroidism
  11 November 2003

  Digital slides
  UI:866 - Bone anomalies of hyperparathyroidism.
  JRC:9408 : Bone changes in hyperparathyroidism (Mandible and maxilla - Hyperparathyroidism)
  Etiology
  familial primary hyperparathyroidism multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A hyperparathyroidism-jaw tumor syndrome (HPT-JT syndrome) familial hypocalciuric hypercalcemia familial isolated hyperparathyroidism
  secondary hyperparathyroidism
  References
  Marx SJ, Simonds WF, Agarwal SK, (...)

• perinatal asphyxia
  19 July 2003

  See also
  perinatal death

• thyroid-associated ophthalmopathy
  12 January 2006

  TAO

• HELLP syndrome
  20 September 2004

  Hemolysis, Elevated Liver enzymes, Low Platelets syndrome WKP
  HELLP syndrome is a life-threatening obstetric complication usually considered to be a variant or complication of pre-eclampsia.
  Both conditions usually occur during the later stages of pregnancy, or sometimes after childbirth. "HELLP" is an abbreviation of the three main features of the syndrome :
  Hemolysis
  Elevated Liver enzymes
  Low Platelet count
  HELLP usually begins during the third trimester; rare cases have (...)

• neonatal hepatic failure
  19 May 2004

  neonatal liver failure

• inherited ataxias
  26 May 2004

  Classification
  autosomal recessive ataxias Friedreich ataxia ataxia telangiectasia sensory ataxias and spinocerebellar ataxias ataxia with isolated vitamin E deficiency abetalipoproteinemia Refsum disease infantile-onset spinocerebellar ataxia ataxia with blindness and deafness cerebellar ataxia with sensory-motor polyneuropathy ataxia with oculomotor apraxia 1 and 2 spinocerebellar ataxia with neuropathy 1 cerebellar ataxias autosomal recessive spastic ataxia of Charlevoix-Saguenay (...)

• cardiogenic shock
  7 December 2005

  Cardiogenic shock results from myocardial pump failure. This may be caused by intrinsic myocardial damage (myocardial infarction), ventricular arrhythmias, extrinsic compression (e.g. cardiac tamponade), or outflow obstruction (e.g. pulmonary embolism).
  See also
  Shock

• TORCH syndrome
  5 January 2005

  TORCH complex, TORCH acronym

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