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Published on: April 21, 2017
An Unusual Presentation of Moyamoya Disease in a Pediatric Patient
Ola Shahrour1, Abdulqader Al Zubaidi2, Salwa Al Kaabi3
1Department of Academic Affairs, Tawam Hospital, Al Ain, ARE.
Abstract:
Moyamoya disease (MMD) is a chronic cerebro-vasculopathy that is extremely rare in the pediatric population. The main characteristic feature is the progressive stenosis in the internal carotid artery with or without the involvement of its main branches in the circle of Willis leading to ischemic stroke. Patients have clinical manifestations related to cerebral ischemia in the carotid branch territories, such as sensory impairment, hemiparesis, and aphasia/dysarthria. Herein, we report a case of MMD in a six-year-old Emirati female who presented with unusual manifestations of MMD in the form of headache, vomiting, and double vision and was diagnosed with MMD based on a brain MRI with angiography. To our knowledge, this is the first reported case of MMD in the United Arab Emirates.
Insights
Moyamoya disease (MMD), a rare pediatric cerebrovascular condition, typically causes stroke. This case highlights unusual MMD symptoms like headache and double vision in a child, presenting a unique diagnostic challenge.
Area of Science:
- Neurology
- Pediatric Neurology
- Vascular Neurology
Background:
- Moyamoya disease (MMD) is a rare chronic cerebrovascular disease affecting children.
- It involves progressive stenosis of the internal carotid artery and circle of Willis branches.
- MMD commonly leads to ischemic stroke with symptoms like hemiparesis and aphasia.
Observation:
- A six-year-old Emirati female presented with atypical MMD symptoms: headache, vomiting, and double vision.
- These symptoms differed from the typical ischemic manifestations of MMD.
- Diagnosis was confirmed via brain MRI with angiography.
Findings:
- The patient was diagnosed with Moyamoya disease.
- This case represents the first reported instance of MMD in the United Arab Emirates.
- The presentation included unusual neurological symptoms in a pediatric patient.
Implications:
- This case expands the understanding of MMD's clinical spectrum in children.
- It emphasizes the importance of considering MMD in pediatric patients with unusual neurological presentations.
- Early diagnosis and management are crucial for improving outcomes in pediatric MMD.
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