Arterial tortuosity syndrome–A case report from Iran
Authors
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.
similar resources
Arterial tortuosity syndrome with multiple intracranial aneurysms: a case report.
OBJECTIVE To report a new manifestation of the rare connective tissue disorder arterial tortuosity syndrome in the absence of skin and soft-tissue abnormalities and with bilateral, giant fusiform intracranial aneurysms. DESIGN Case report. SETTING University teaching hospital. PATIENT A 67-year-old man with a history of hypertension presented to medical attention after a syncopal episode....
full textArterial tortuosity syndrome.
To cite: Mehrabi E, Khan K, Malik SA. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2016217029 DESCRIPTION An infant exhibited weight faltering and failure to thrive after birth. She was born full term via an uncomplicated vaginal delivery to healthy, nonconsanguineous parents. The mother received prenatal care and standard screening tests were reportedly normal...
full textCardiovascular findings in a boy with arterial tortuosity syndrome: case report and review of the literature.
Arterial tortuosity syndrome (ATS) is a rare hereditary, autosomal recessive, connective tissue disorder. Herein, we describe a five-year-old boy. He had hyperextensible skin, atypical facial features and inguinal hernia. We present his vascular imaging studies of kinking and tortuosity of the aorta and bilateral multiple peripheral pulmonary artery stenoses determined by conventional and magne...
full textEpilepsy as the first presentation of arterial tortuosity syndrome in a young girl: a case report.
Arterial tortuosity syndrome (ATS) is an extremely rare autosomal recessive connective tissue disorder characterized by tortuosity and elongation of all major arteries. We report a clinical case of a girl with this rare condition, who initially presented with epilepsy. DSA or MRA revealed a severe arterial tortuosity. EEG showed epileptiform discharge in right frontotemporal hemisphere. Here, w...
full textHybrid approach in a case of arterial tortuosity syndrome.
Arterial tortuosity syndrome is a rare connective tissue disorder characterised by elongation, tortuosity, stenosis and aneurysms of the large and middle-sized arteries. The symptomatology is correlated to the artery affected by the pathology with correlated stenosis. We describe our hybrid surgical procedure in the treatment of a case of kinking of the pulmonary branches with significant gradi...
full textA Case of Carotid Aneurysm in Familial Retinal Arterial Tortuosity
A 44-year-old woman who showed recurrent vitreous hemorrhages with vascular tortuosity received CT angiography which revealed an internal carotid artery aneurysm. A case of internal carotid aneurysm was associated with a pattern of retinal arteriolar tortuosity pathognomic for familial retinal arterial tortuosity (fRAT), suggesting possible involvement of the cerebral circulation. We present a ...
full textMy Resources
Journal title
volume 1 issue None
pages 28- 30
publication date 2015-03
By following a journal you will be notified via email when a new issue of this journal is published.
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023