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Lysinuric protein intolerance
Lysinuric protein intolerance: Introduction
Lysinuric protein intolerance: A rare inborn urea cycle disorder characterized by an enzyme defect in the amino acid transporter gene SLC7A7 (positive amino acid transporter). More detailed information about the symptoms, causes, and treatments of Lysinuric protein intolerance is available below.
Symptoms of Lysinuric protein intolerance
Read more about symptoms of Lysinuric protein intolerance
Lysinuric protein intolerance: Complications
Read more about complications of Lysinuric protein intolerance.
Causes of Lysinuric protein intolerance
Read more about causes of Lysinuric protein intolerance.
Evidence Based Medicine Research for Lysinuric protein intolerance
Medical research articles related to Lysinuric protein intolerance include:
- Haemophagocytic syndrome
- Children's Interstitial Lung Disease (ChILD) (Diagnosis)
- April 2007 Update
- Carnitine Deficiency (Follow-up)
- Aminoacidurias
- Carnitine Deficiency (Diagnosis)
- more research...»
Click here to find more evidence-based articles on the TRIP Database
Videos for Lysinuric protein intolerance
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Reseach about Lysinuric protein intolerance
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Definitions of Lysinuric protein intolerance:
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Lysinuric protein intolerance as a "rare disease".
Source - Orphanet
- Lysinuric protein intolerance
- What is Lysinuric protein intolerance?
- Prevalence and Incidence of Lysinuric protein intolerance
- Videos related to Lysinuric protein intolerance
- Causes of Lysinuric protein intolerance
- Symptoms of Lysinuric protein intolerance
- Signs of Lysinuric protein intolerance
- Complications of Lysinuric protein intolerance
- Treatments for Lysinuric protein intolerance
- Cure Research for Lysinuric protein intolerance
- Glossary for Lysinuric protein intolerance
- External links relating to Lysinuric protein intolerance
- Milk Protein Intolerance (The 5-Minute Pediatric Consult)
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