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{{Endocardial cushion defect}}
{{Endocardial cushion defect}}
{{CMG}} ; {{AE}} {{ADG}}
{{CMG}} ; {{AE}} {{ADG}} <br>
{{SK}} Atrioventricular septal defect; atrioventricular canal defect; AV canal defect; AV septal defects; canalis atrioventricularis communis; persistent atrioventricular ostium; abnormal development of endocardial cushions
{{SK}} Atrioventricular septal defect; atrioventricular canal defect; AV canal defect; AV septal defects; canalis atrioventricularis communis; persistent atrioventricular ostium; abnormal development of endocardial cushions



Revision as of 22:37, 6 June 2020

Endocardial cushion defect Microchapters

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Overview

Classification

Pathophysiology

Causes

Differentiating Endocardial cushion defect from other Diseases

Epidemiology and Demographics

Risk Factors

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Natural History, Complications and Prognosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Aditya Ganti M.B.B.S. [2]
Synonyms and keywords: Atrioventricular septal defect; atrioventricular canal defect; AV canal defect; AV septal defects; canalis atrioventricularis communis; persistent atrioventricular ostium; abnormal development of endocardial cushions

Overview

Historical Perspective

Classification

Based on the anatomical features and their impact on physiology, endocardial cushion defect may be classified into complete, partial, intermediate, transitional, and intermediate forms.

Pathophysiology

AV canal connects the atria to the ventricles. At four to five weeks of gestation, the superior and inferior endocardial cushions of the common AV canal fuse. Results in the formation of the mitral and tricuspid valve and the AV septum. Any failure of fusion results in endocardial cushion defect. Pathophysiology of endocardial cushion defects depends upon level of left to right shunting and degree of shunting. Incompetent AV valves in endocardial cushion defect results in regurgitation. There is a strong association between AV canal defects and Down syndrome

Causes

Differentiating Xyz from Other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications, and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

References


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