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The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 1361
Carnosinemia is a very rare inherited disorder that presents with serum carnosinase deficiency.
About 30 individuals have been reported worldwide.
The gene associated with this disease has not been identified. The majority of the patients showed variable degrees of intellectual deficit. Some patients had seizures and one had congenital myopathy. A few patients had no symptoms at all.
Diagnosis is based on amino acid analysis of serum and/or urine after exclusion of meat from the diet, and enzymatic testing.
The differential diagnosis includes gamma-amino butyric acid (GABA) transaminase deficiency.
Autosomal recessive inheritance has been suggested.
Management and treatment
No efficient treatment is available, and it remains uncertain whether treatment is necessary.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
80%-99% of people have these symptoms.
Click on a symptom to see definitions for associated terms.
|Olfactory lobe agenesis|
|Generalized myoclonic seizures|
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