Rare association of anophthalmia, complex congenital heart disease and pulmonary hypertension: case report

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Evaluation of QRS, QTc, and JTc intervals in Congenital Heart Disease with Pulmonary Hypertension

Background Pulmonary hypertension (PH) in congenital heart disease affects the patient’s prognosis. Prolonged QRS and QTc intervals in ECG may intensify life-threatening dysrhythmia in patients. We aimed to investigate the correlation between QRS, QTc, and JTc intervals prolongation in ECG with PH in Congenital Heart Disease (CHD) patients. Mate...

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[Anophthalmia and congenital cataract: case report].

The authors report a case of anophthalmia, congenital cataract and systemic malformations. Male patient, 6 months old, left anophthalmia and congenital posterior polar cataract in the right eye. The patient was treated with manual aspiration of the crystalline lens, with no intraocular lens implantation with primary posterior capsulorhexis and anterior vitrectomy through a small incision. The a...

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Congenital heart disease and pulmonary hypertension.

Many patients with congenital heart disease and systemic-to-pulmonary shunts develop pulmonary arterial hypertension (PAH), particularly if the cardiac defect is left unrepaired. A persistent increase in pulmonary blood flow may lead to obstructive arteriopathy and increased pulmonary vascular resistance, a condition that can lead to reversal of shunt and cyanosis (Eisenmenger syndrome). Cardia...

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Congenital Heart Disease and Pulmonary Hypertension

Pulmonary hypertension is common in patients with congenital heart disease, even in those patients with previously repaired lesions, and can lead to considerable symptoms, including exertional dyspnea. Pulmonary hypertension in these patients can be caused by pulmonary arterial or pulmonary venous causes and requires heart catheterization for accurate diagnosis. Some patients may be able to be ...

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ژورنال

عنوان ژورنال: Medwave

سال: 2016

ISSN: 0717-6384

DOI: 10.5867/medwave.2016.09.6568