Beta ketothiolase deficiency
Beta ketothiolase deficiency: Introduction
Beta ketothiolase deficiency: A rare inherited disease characterized by the bodies inability to metabolise certain amino acids and products of the breakdown of fat. Harmful levels of organic acids build up in the body and cause ketoacidic attacks.
More detailed information about the symptoms,
causes, and treatments of Beta ketothiolase deficiency is available below.
Symptoms of Beta ketothiolase deficiency
See full list of 9
symptoms of Beta ketothiolase deficiency
Wrongly Diagnosed with Beta ketothiolase deficiency?
Beta ketothiolase deficiency: Related Patient Stories
Beta ketothiolase deficiency: Deaths
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Beta ketothiolase deficiency: Complications
Review possible medical complications related to Beta ketothiolase deficiency:
Causes of Beta ketothiolase deficiency
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More information about causes of Beta ketothiolase deficiency:
Disease Topics Related To Beta ketothiolase deficiency
Research the causes of these diseases that are similar to, or related to, Beta ketothiolase deficiency:
Less Common Symptoms of Beta ketothiolase deficiency
Read more about symptoms of Beta ketothiolase deficiency
Misdiagnosis and Beta ketothiolase deficiency
Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency
is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis).
See ...read more »
Read more about Misdiagnosis and Beta ketothiolase deficiency
Statistics for Beta ketothiolase deficiency
Beta ketothiolase deficiency: Broader Related Topics
Types of Beta ketothiolase deficiency
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Definitions of Beta ketothiolase deficiency:
Beta ketothiolase deficiency is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Beta ketothiolase deficiency, or a subtype of Beta ketothiolase deficiency,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Beta ketothiolase deficiency as a "rare disease".
Source - Orphanet
Contents for Beta ketothiolase deficiency: