Krabbé Disease: Brain myelin disorder with various symptoms. More detailed information about the symptoms, causes, and treatments of Krabbé Disease is available below.
See full list of 8 symptoms of Krabbé Disease
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Prognosis for Krabbé Disease: poor. Typically fatal by age 2.
More about prognosis of Krabbé Disease
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The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
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A degenerative disease of the central and peripheral nervous system caused by abnormal breakdown and turnover of myelin and marked by reduced galacosylceramide beta-galactosidase activity (EC 3.2.1.46). Two types based on the age of onset are recognized: Infantile-onset Krabbe disease is marked by the appearance of symptoms at ages 3-6 months, which include irritability, frequent crying, and increase of muscle tonus. They are followed by opisthotonos, less of tendon reflexes, visual failure, elevated cerebrospinal fluid proteins, and delayed nerve conduction velocity. Most infants die during the second year of life. Late-onset Krabbe disease (LOKD) has first symptoms at ages 5 to 10 years, consisting of focal neurological signs, hemiparesis, cerebellar ataxia, cortical blindness, and spastic paraplegia, followed by mental and physical deterioration. Some patients survive into adulthood. - (Source - Diseases Database)
Krabbé Disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Krabbé Disease, or a subtype of Krabbé Disease,
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 Krabbé Disease as a "rare disease".
Source - Orphanet
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