DISEASE DIRECTORY

Wednesday, January 07, 2009

Rare Disorders

 Agnosia
Aicardi Syndrome
Alstrom Syndrome
Barth Syndrome
Cerebrocostomandibular Syndrome
Cleidocranial Dysplasia
Cystinosis
Degos
Erythromelalgia
Jacobsen Syndrome
Melorheostosis
Moyamoya
Ollier Disease
Pemphigoid
Pemphigus
Phenylketonuria
Pierre Robin Syndrome
Progeria
Rubinstein-Taybi Syndrome
Tyrosinemia
VATER Syndrome
Wegener's Granulomatosis

  • 11. Tyrosinemia - Page 1. 7/02 NBS99 140 11. Tyrosinemia 11.0 Introduction Screening for tyrosinemia is now formally included in only a few screening programs.
  • 11. Tyrosinemia - Page 1. 02/03 NBS 2000 140 11. Tyrosinemia 11.0 Introduction Screening for tyrosinemia is now formally included in only a few screening programs.
  • Conditions and Diseases - Tyrosinemia Top Links - Tyrosinemia Web Site Links. NORD - Tyrosinemia, Hereditary - Offers the synonyms, a general discussion and further resources. Pediatric
  • Geometry.Net - Health_Conditions: Tyrosinemia - Tyrosinemia Information about tyrosinemia, a rare metabolic disorder. This is the place for all people interested in connecting with others with Tyrosinemia.
  • Hereditary Tyrosinemia - The two most common inborn errors of tyrosine catabolism are hepatorenal tyrosinemia (tyrosinemia type I) and oculocutaneous tyrosinemia (tyrosinemia type II).
  • National Library of Medicine - The synonyms of Tyrosinemia 11, a summary and major features.
  • Newborn Screening Program - Tyrosinemia - Tyrosinemia. Definition. The tyrosinemias Newborn screening in Illinois includes testing for the following type of tyrosinemia: Tyrosinemia type
  • NORD: Ollier Disease - Sample report, plus links to organisations. [Fee required for full report]
  • Paul and Erich Lauffs: Tyrosinemia - The American Liver Foundation - Tyrosinemia They decided to go ahead, and Colleen had amniocentesis. When the results of tests were negative for tyrosinemia, the ecstatic family celebrated.
  • Pediatric Database - Offers a definition of Tyrosinemia-1, the epidemiology, pathogenesis, clinical features, investigations and management.
  • SearchBug Open Directory -> Health -> Conditions_and_Diseases ... - Open Directory. Search: Tyrosinemia, Tyrosinemia Group - http://groups.msn.com/tyrosinemia Information about tyrosinemia, a rare metabolic disorder.
  • Tyrosinemia - [ Home ] [ Up ]. Click Here! Tyrosinemia. Click Here! Music-e.net Just-recipes.net EnvyMag.com Scholarships-4u.com Shesearch.com Free
  • Tyrosinemia - Advertisement. Tyrosinemia Guide picks. Tyrosinemia Type I Article describes the disorder, its symptoms, diagnosis, and treatment.
  • TYROSINEMIA - Hereditary tyrosinemia is a genetic inborn error of metabolism associated with severe liver disease in infancy. The disease is inherited
  • Tyrosinemia - More Tyrosinemia Categories: » Submit Your Site to the Tyrosinemia category. Submit Your Site to the Tyrosinemia category. Featured Partner.
  • Tyrosinemia - For all people interested in connecting with others with this disease.
  • TYROSINEMIA - Definition by HyperDictionary.com - Hyper Dictionary. English Dictionary, Computer Dictionary, Thesaurus, Dream Dictionary, Medical Dictionary. Search Dictionary: TYROSINEMIA. WordNet Dictionary.
  • Tyrosinemia - Liver Health Information - The American Liver ... - Tyrosinemia, Hereditary tyrosinemia is a genetic inborn error of metabolism associated with severe liver disease in infancy. The
  • tyrosinemia -- Encyclopædia Britannica - Encyclopædia Britannica, tyrosinemia Encyclopædia Britannica Article. This enzyme is not active in individuals with tyrosinemia. Clinical….
  • Tyrosinemia Group - Information about tyrosinemia, a rare metabolic disorder. Includes lists of links to other support groups, sources for low protein food, recipes, message board.
  • Tyrosinemia Information - home > rare disorders > tyrosinemia Tyrosinemia. Web Directory: ? National Library of Medicine The synonyms of Tyrosinemia 11, a summary and major features.
  • TYROSINEMIA TYPE II: REPORT OF THE FIRST FOUR CASES IN SAUDI ... - 466 Annals of Saudi Medicine, Vol 18, No 5, 1998 TYROSINEMIA TYPE II: REPORT OF THE FIRST FOUR CASES IN SAUDI ARABIA M. Al-Essa, MD; M. Rashed, PhD; PT Ozand
  • Tyrosinemia, Hereditary - Tyrosinemia type I is a rare genetic metabolic disorder characterized by lack of the enzyme fumarylacetoacetate hydrolase (FAH), which is needed to break down
  • Tyrosinemia-11 - An in depth look at this disease from Pediatric Database including investigations and management.