Title of article :
Arterial tortuosity syndrome–A case report from Iran
Author/Authors :
Zamani، Hassan Ali نويسنده Department of Applied Chemistry, Islamic Azad University, Quchan branch, Quchan, Iran , , Goodarzi، Mohammad نويسنده Gorgan University of Medical sciences Goodarzi, Mohammad , Babazadeh ، Kazem نويسنده Non-Communicable Pediatric Diseases Research Center, Babol University of Medical Sciences, Babol, Iran. , , Mirzapour، Mohaddese نويسنده Faculty of Traditional Iranian Medicine Mirzapour, Mohaddese
Issue Information :
دوفصلنامه با شماره پیاپی 1 سال 2015
Pages :
3
From page :
28
To page :
30
Abstract :
Introduction: Arterial tortuosity syndrome (ATS), an autosomal recessive rare connective tissue disorder characterized by tortuosity, elongation and stenosis in the large and medium sized arteries. It manifestations include vascular and nonvascular connective tissue related symptoms. In this literature we describe the first cases of ATS from Iran. Case report: A six-months-old female was presented with a heart murmur in the right upper sternal edge that was followed up for diaphragmatic hernia repair. Positive sign include right axis deviation in electrocardiography (ECG), abnormal long and tortuous aortic arch with tortuosity of its branches in angiography, increased right ventricular pressure up to 60 mmHg and slight right ventricular hypertrophy with severe stenosis of pulmonary artery bifurcation. Conclusions: ATS does not present with a unique set of clinical features and its manifestations depend on the mutation type. The most common presentation is tortuous artery and more report of this rare case can help to better diagnosis of ATS.
Journal title :
Caspian Journal of Pediatrics
Serial Year :
2015
Journal title :
Caspian Journal of Pediatrics
Record number :
2391259
Link To Document :
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