Tricuspid atresia history and symptoms: Difference between revisions
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==History and Symptoms== | ==History and Symptoms== | ||
The patients commonly have a history of [[ cyanosis]] and symptoms of[[ heart failure]] from the birth time. | The patients commonly have a history of [[ cyanosis]] and symptoms of [[ heart failure]] from the birth time. | ||
==Symptoms== | ==Symptoms== | ||
Latest revision as of 16:30, 8 November 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor-In-Chief: Sara Zand, M.D.[2] Keri Shafer, M.D. [3] Priyamvada Singh, MBBS [4] Assistant Editor-In-Chief: Kristin Feeney, B.S. [5]
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History and Symptoms
The patients commonly have a history of cyanosis and symptoms of heart failure from the birth time.
Symptoms
Symptoms of tricuspid atresia in neonates may include the following:[1]
- Central cyanosis in mucous membranes and tongue
- Poor feeding and growth retardation
- Difficulty in breathing
- Rapidheartbeats
- Rapid breathing
Symptoms of longstanding cyanosis and hyperviscosity syndrome as a result of secondary erythrocytosis in older children include the following:
References
- ↑ Rao, P. Syamasundar (2009). "Diagnosis and management of cyanotic congenital heart disease: Part I". The Indian Journal of Pediatrics. 76 (1): 57–70. doi:10.1007/s12098-009-0030-4. ISSN 0019-5456.