Neurovascular Manifestation of Loeys-Dietz Syndrome: A Case Report

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Neurovascular Manifestation of Loeys-Dietz Syndrome: A Case Report

A 5-year-old boy was referred to our hospital for evaluation of headache, tortuous intracranial arteries and vertebral arteries found up on brain magnetic resonance angiography. The patient’s family history was unremarkable for any genetic disease. He was born at 39 weeks of gestation by spontaneous vaginal delivery without complications. His birth weight was 3,580 gm. At 3 years Neurovascular ...

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Neuroradiologic Manifestations of Loeys - Dietz Syndrome Type

V.J. Rodrigues S. Elsayed B.L. Loeys H.C. Dietz D.M. Yousem BACKGROUND AND PURPOSE: Loeys-Dietz syndrome (LDS) is a recently described entity that has the triad of arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate. Its neuroradiologic manifestations have not been well delineated. We sought to describe the neuroradiologic features of LDS and to assess the manifest...

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Loeys-Dietz syndrome in pregnancy: a case description and report of a novel mutation.

Loeys-Dietz syndrome is a syndrome caused by heterozygous mutations in the genes encoding type 1 or 2 transforming growth factor-beta receptor (TGF-beta-R1/2). The obstetrical manifestations are risk of rupture of the gravid uterus and the arteries, either during pregnancy or in the immediate postpartum period, and damage to the vagina, perineum and the colon. We describe, for the first time, a...

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Loeys-Dietz syndrome with bilateral radial head dislocations: a case report.

Loeys-Dietz syndrome is characterised by vascular aneurysms, hypertelorism, and a bifid uvula. We report on an 11-year-old boy with Loeys-Dietz syndrome who presented with bilateral radial head dislocations and severe osteopaenia with changes of avascular necrosis in both hips causing an out-toeing, wide gait. Considering the poor prognosis for elbow movement and possible radial head dysplasia,...

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CASE REPORT Cerebral arterial angioplasty in a patient with Loeys–Dietz syndrome

To cite: Kellner CP, Sussman ES, Donaldson C, et al. J NeuroIntervent Surg 2015;7:e2. ABSTRACT A 14-year-old boy with Loeys–Dietz syndrome (LDS) had an acute neurologic decline 6 days after a subarachnoid hemorrhage. Cerebral angiography at presentation did not show an aneurysmal source of the hemorrhage. However, on post-bleed day 6 the patient experienced an acutely worsening headache and sub...

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ژورنال

عنوان ژورنال: Journal of Genetic Medicine

سال: 2013

ISSN: 1226-1769,2383-8442

DOI: 10.5734/jgm.2013.10.1.47