A 45 years old male was admitted to the ER with sudden muscle weakness and facial paralysis on the left side. The patient’s history consists of intermittent claudication without any treatment. The patient’s vitals show no abnormalities except for high blood pressure with 159/80 mmHg. The patient’s brain CT scan shows acute infarction in the right cerebral hemisphere suggesting right middle cerebral artery infarction. Computed tomography angiography shows severe stenosis of the right internal carotid artery, infarction of the M1 section of the right middle cerebral artery. Cardiosonography reveals mild mitral stenosis, moderate tricuspid regurgitation 2/4, and mild pulmonary artery hypertension. Carotid artery Doppler ultrasound remarks a large atherosclerotic plaque in the right carotid bifurcation and right internal carotid artery that block more than 50% of the right carotid artery. Carotid artery Doppler ultrasound also reveals left subclavian steal syndrome and multiple stenoses as well as atherosclerosis in common carotid arteries, left internal carotid artery, external carotid artery, right vertebral artery, and right subclavian artery. Incidentally, abdominal aorta Doppler ultrasound found a chronic abdominal aortic occlusion at the location from left renal artery to bilateral external iliac arteries. Lower extremities Doppler ultrasound shows normal circulation received mostly from collateral circulation from deep femoral arteries. However, as the priority at the time was to resolve the patient’s cerebral artery stroke, and no immediate renal failure or reduced blood flow to the lower limb was noted, we decided to delay any work-up regarding the abdominal aorta.

Emergency management for this patient was to re-establishment of the cerebral circulation. The patient at the time of hospitalization met the requirements for using of tissue plasminogen activator. The patient was administered Alteplase with the dose of 0.9 mg/kg and transferred to Interventional Cardiovascular Unit for mechanical thrombectomy with a Solitaire device under the guide of digital subtraction angiography (DSA). Post-intervention, the patient achieved a score of 3 using modified treatment in cerebral ischemia (mTICI) score.

The patient was transferred to the Department of Cardiology on the following day. An angiogram of the patient’s abdominal aorta was taken using sheath 8F with right brachial artery insertion. The angiogram shows complete occlusion of the abdominal aorta at the level of 10 mm above aortic bifurcation, with no abnormalities in internal and external iliac arteries, except for 50% narrowing in the left external iliac artery and occlusion in the distal section of the left internal iliac artery. As the patient presented with no apparent renal insufficiency or lower limb ischemia, after weighing in the risk and benefit, the decision to reverse the mid-aortic occlusion was postponed indefinitely and the patient were scheduled for regular check-up.

The patient was discharged 1 week later in good condition and with full recovery of limb mobility and no apparent sequelae of stroke was noted upon subsequent visit.

Blood samples were collected for genetic workup. In this patient, karyotyping and CNV analysis further revealed XXY aneuploidy, the patient had no children and was suspected of low fertility due to Klinefelter syndrome. However, the XXY aneuploidy has not been attributable to mid-aortic syndrome therefore we suspected a monogenic cause. Whole Exome sequencing (GeneSolution, Ho Chi Minh City, Vietnam) was conducted for this patient, data analysis focused on genes related to cardiovascular diseases and connective tissue disorders. The result revealed a variant at the ELN gene (Elastin, OMIM*130,160): c.1768G > A/wt (p.Ala590Thr). To assess the pathogenicity and any previously reported pathogenic variant of ELN, we used Human Gene Mutation Database, LOVD, ClinVar as reference databases and followed American College of Medical Genetics (ACMG) Guidelines for interpretation of pathogenic variant [6]. The variant was observed at a very low frequency in the general population and the Asian population at a frequency of 0.000012 (Genome Aggregation Database March 6, 2019, v2.1.1), this variant was not previously reported in patients with Mid-aortic syndrome, and the ACMG verdict was “Likely Pathogenic”.