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Condition

Tricuspid atresia

Congenital Malformations and Chromosomal Abnormalities

Tricuspid atresia is a form of congenital heart disease in which there is a complete absence of the tricuspid valve. This defect prevents blood flow between the right atrium and right ventricle, resulting in an undersized right ventricle and deoxygenated blood circulating through the body. The causes of tricuspid atresia are unknown; the condition develops during prenatal heart development when the tricuspid valve fails to form properly. Early signs include progressive skin discoloration from poor oxygenation, feeding difficulties, and rapid breathing within the first two weeks of life. Physical examination typically reveals heart murmurs and abnormal heart sounds, and electrocardiography shows left axis deviation and enlarged left heart chambers, since the left ventricle must pump blood to both the pulmonary and systemic circulations in the absence of a functioning right ventricle.

Facts
Classification
Body System
Cardiovascular System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Communicable or Non-communicable
Non-Communicable 1
Transmission Route
Non-Transmissible 1
Causative Agent
Causative Agent (category)
Idiopathic / Multifactorial 1
Connections

Treated By

Source Wikidata: Glenn Procedure
Sources
1. Tricuspid atresia (Wikipedia)
Wikipedia intro: Tricuspid atresia: congenital heart disease, 'causes of tricuspid atresia are unknown'View the Source
2. Wikidata: Tricuspid atresia
Wikidata P494 (Q22.4)View the Source
Wikidata: Glenn Procedure
Treated By: Glenn Procedure, lead paragraphView the Source
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