What does this research mean for the field?

Suspected right ventricular dysplasia in an infant can present with unique angiocardiographic features, including outpouchings resembling multiple diverticula in both ventricles, and is associated with a high risk of sudden death. Novelty: ClaimNovelty.NOVEL_FINDING. Consensus alignment: ConsensusAlignment.NEUTRAL.

January 1, 1988Clinical CardiologyOpen Access

An infant with suspected right ventricular dysplasia presenting unique ventriculograms

View Full Paper

Ask AI

Bookmark

Population

1 male infant with suspected right ventricular dysplasia presenting with cyanosis during crying at 10 days…

Design

Case_report

Follow-up

4 years and 10 months

Authors

YMYuji Matsuoka KKKenji Kawaguchi TOTakahiro Okishima

Discussion

Member takes

Overview

May signal high sudden-death risk in infants with ventricular outpouchings; leaves open whether these represent a distinct cardiomyopathy subtype.

Structured PICO

Population

1 male infant with suspected right ventricular dysplasia presenting with cyanosis during crying at 10 days after birth and evaluated at 4 years and 10 months of age

Intervention

Angiocardiography, echocardiography, and electrocardiography

Outcome

Angiocardiographic findings and clinical course

This case report describes unique angiocardiographic findings of multiple diverticula-like outpouchings in an infant with suspected right ventricular dysplasia who suffered sudden cardiac death.

Limitations

No autopsy performed, so definitive diagnosis could not be made

Cite This Study

Matsuoka et al. (1988) studied this question.

synapsesocial.com/papers/6a189b3d0048a5c8b24aaa60 https://doi.org/10.1002/clc.4960110119

View Full Paper

Ask AI

Bookmark

January 1, 1988Clinical CardiologyOpen Access

An infant with suspected right ventricular dysplasia presenting unique ventriculograms

View Full Paper

Ask AI

Bookmark

Population

1 male infant with suspected right ventricular dysplasia presenting with cyanosis during crying at 10 days…

Design

Case_report

Follow-up

4 years and 10 months

Authors

YMYuji Matsuoka KKKenji Kawaguchi TOTakahiro Okishima

Discussion

Member takes

Overview

May signal high sudden-death risk in infants with ventricular outpouchings; leaves open whether these represent a distinct cardiomyopathy subtype.

Structured PICO

Population

1 male infant with suspected right ventricular dysplasia presenting with cyanosis during crying at 10 days after birth and evaluated at 4 years and 10 months of age

Intervention

Angiocardiography, echocardiography, and electrocardiography

Outcome

Angiocardiographic findings and clinical course

This case report describes unique angiocardiographic findings of multiple diverticula-like outpouchings in an infant with suspected right ventricular dysplasia who suffered sudden cardiac death.

Limitations

No autopsy performed, so definitive diagnosis could not be made

Cite This Study

Matsuoka et al. (1988) studied this question.

synapsesocial.com/papers/6a189b3d0048a5c8b24aaa60 https://doi.org/10.1002/clc.4960110119

View Full Paper

Ask AI

Bookmark