1983
DOI: 10.1136/hrt.50.1.31
|View full text |Cite
|
Sign up to set email alerts
|

Congenital absence of pulmonary valve leaflets.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
1
0
2

Year Published

1986
1986
2014
2014

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 14 publications
(3 citation statements)
references
References 36 publications
0
1
0
2
Order By: Relevance
“…The presence of incomplete right bundle branch block associated with right ventricular hypertrophy, as present in our case, can be of value in differentiating congenital APV from TOF. 4 Either pulmonary air entrapment with emphysema or atelectasis may result from the obstruction of the respective bronchus resulting from compression by the dilated pulmonary artery branches. Gross dilatation of the pulmonary artery and its branches with an abrupt transition in caliber between the main trunks and their immediate branches is typical of this malformation.…”
Section: Discussionmentioning
confidence: 99%
“…The presence of incomplete right bundle branch block associated with right ventricular hypertrophy, as present in our case, can be of value in differentiating congenital APV from TOF. 4 Either pulmonary air entrapment with emphysema or atelectasis may result from the obstruction of the respective bronchus resulting from compression by the dilated pulmonary artery branches. Gross dilatation of the pulmonary artery and its branches with an abrupt transition in caliber between the main trunks and their immediate branches is typical of this malformation.…”
Section: Discussionmentioning
confidence: 99%
“…Las radiografias de torax generalmente muestran cardiomegalia moderada, pero tambien han sido descritos casos con silueta cardiaca de tamano normal. La cardiomegalia ha sido relacionada con la severidad de la regurgitacion pulmonar 37 . La dilatacion de la arteria pulmonar se puede observar claramente en la proyeccion frontal, y la arteria pulmonar izquierda, puede identificarse mas facilmente en la proyeccion oblicua izquierda anterior.…”
Section: D1scusionunclassified
“…Esta rara malformacion cardiaca muy pocas veces se manifiesta como una lesion aislada: unicamente 6 casos han sido descritos 8 " 13 . Lo habitual es que se asocie a otras anomalies, mas frecuentemente tetralogi'a de Fallot 13 " 21 o CIV con o sin estenosis infundibular pulmonar, dando origen a un sindrome bastante caracterfstico 3 - 4 ' 13, 22-27 Hasta { a fecha 289 casos han sido publicados 13 -34 « 36 - 37 .…”
unclassified