Prenatal diagnosis of isolated tricuspid valve atresia: Report of 4 cases and review of the literature

Objective. To describe the prenatal features of fetal tricuspid atresia. Methods. Four cases of fetal tricuspid atresia were prenatally diagnosed, sonographically described, and followed. Results. On the basis of this small series, the key findings for diagnosis included the demonstration of no pate...

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Main Authors: Tongsong T., Sittiwangkul R., Wanapirak C., Chanprapaph P.
Format: Review
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-3142677869&partnerID=40&md5=4e4e4b93fcfd52ebdf28efaf28f05ecb
http://www.ncbi.nlm.nih.gov/pubmed/15292563
http://cmuir.cmu.ac.th/handle/6653943832/4012
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-40122014-08-30T02:35:34Z Prenatal diagnosis of isolated tricuspid valve atresia: Report of 4 cases and review of the literature Tongsong T. Sittiwangkul R. Wanapirak C. Chanprapaph P. Objective. To describe the prenatal features of fetal tricuspid atresia. Methods. Four cases of fetal tricuspid atresia were prenatally diagnosed, sonographically described, and followed. Results. On the basis of this small series, the key findings for diagnosis included the demonstration of no patent tricuspid valve on the 4-chamber view, no flow across the tricuspid valve on pulsed or color Doppler flow mapping, small right ventricles, and associated interventricular septal defects. Increased nuchal translucency thickness may give the first clue leading to follow-up scans, resulting in a definite diagnosis. Conclusions. Tricuspid atresia can be readily diagnosed prenatally. The key findings and differential diagnoses are provided. 2014-08-30T02:35:34Z 2014-08-30T02:35:34Z 2004 Review 02784297 15292563 JUMED http://www.scopus.com/inward/record.url?eid=2-s2.0-3142677869&partnerID=40&md5=4e4e4b93fcfd52ebdf28efaf28f05ecb http://www.ncbi.nlm.nih.gov/pubmed/15292563 http://cmuir.cmu.ac.th/handle/6653943832/4012 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Objective. To describe the prenatal features of fetal tricuspid atresia. Methods. Four cases of fetal tricuspid atresia were prenatally diagnosed, sonographically described, and followed. Results. On the basis of this small series, the key findings for diagnosis included the demonstration of no patent tricuspid valve on the 4-chamber view, no flow across the tricuspid valve on pulsed or color Doppler flow mapping, small right ventricles, and associated interventricular septal defects. Increased nuchal translucency thickness may give the first clue leading to follow-up scans, resulting in a definite diagnosis. Conclusions. Tricuspid atresia can be readily diagnosed prenatally. The key findings and differential diagnoses are provided.
format Review
author Tongsong T.
Sittiwangkul R.
Wanapirak C.
Chanprapaph P.
spellingShingle Tongsong T.
Sittiwangkul R.
Wanapirak C.
Chanprapaph P.
Prenatal diagnosis of isolated tricuspid valve atresia: Report of 4 cases and review of the literature
author_facet Tongsong T.
Sittiwangkul R.
Wanapirak C.
Chanprapaph P.
author_sort Tongsong T.
title Prenatal diagnosis of isolated tricuspid valve atresia: Report of 4 cases and review of the literature
title_short Prenatal diagnosis of isolated tricuspid valve atresia: Report of 4 cases and review of the literature
title_full Prenatal diagnosis of isolated tricuspid valve atresia: Report of 4 cases and review of the literature
title_fullStr Prenatal diagnosis of isolated tricuspid valve atresia: Report of 4 cases and review of the literature
title_full_unstemmed Prenatal diagnosis of isolated tricuspid valve atresia: Report of 4 cases and review of the literature
title_sort prenatal diagnosis of isolated tricuspid valve atresia: report of 4 cases and review of the literature
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-3142677869&partnerID=40&md5=4e4e4b93fcfd52ebdf28efaf28f05ecb
http://www.ncbi.nlm.nih.gov/pubmed/15292563
http://cmuir.cmu.ac.th/handle/6653943832/4012
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