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Jacobsen syndrome (medical condition): A very rare chromosomal disorder involving the absence of a portion of chromosome 11q. The range and severity of symptoms is determined by the size of the portion that is deleted.
See also:
Jacobsen syndrome:
»Introduction: Jacobsen syndrome
»Symptoms of Jacobsen syndrome
»Treatments for Jacobsen syndrome
Jacobsen syndrome: Deletion of the long arm of chromosome 11 with retarded growth and psychomotor development, trigonocephaly, strabismus, short and broad nose with anteverted nostrils, epicanthus, telecanthus, malformed ears, "carp mouth", camptodactyly, and thrombocytopenia.
Source: Diseases Database
Jacobsen syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Jacobsen syndrome, or a subtype of Jacobsen syndrome,
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 if affects 1 person per 2,000.
They list Jacobsen syndrome as a "rare disease".
Source - Orphanet
Jacobsen syndrome (medical condition): See Jacobsen syndrome (disease information).
»Introduction: Jacobsen syndrome
»Symptoms of Jacobsen syndrome
»Treatments for Jacobsen syndrome
Source: Diseases Database
Source - NIH
Source: Diseases Database
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