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Erondu-Cymet syndrome

Congenital Malformations and Chromosomal Abnormalities

Erondu-Cymet syndrome, discovered in 2006 by Ugochi Erondu and Tyler Cymet, is a condition caused by a translocation on chromosome 21 that produces low blood pressure, reduced blood oxygen, seizures, cognitive impairment, and cardiovascular abnormalities including a persistent left superior vena cava and pulmonary arteriovenous malformations.

Facts
Classification
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 1
Communicable or Non-communicable
Non-Communicable 2
Transmission Route
Non-Transmissible 2
Causative Agent
Causative Agent (category)
Genetic / Hereditary 3
First Described
2006 3
Sources
1. Wikipedia: ICD-10
WikipediaList of chapters, Chapter XVII
Quote, List of chapters, Chapter XVII
Congenital malformations, deformations and chromosomal abnormalities
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2. Wikipedia: Non-communicable disease
Wikipedia
  • Lead section, transmission-route statement (inferred from disease-category)
    Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
  • Inherited/genetic diseases section
    Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
View the Source
3. Erondu-Cymet syndrome (Wikipedia)
Discovered in 2006 by Ugochi Erondu and Tyler Cymet, article introView the Source
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