ArticleInternational medical case reports journal2022
A Rare Case of Dandy-Walker Syndrome.
Article in International medical case reports journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 8 citations in OpenAlex.
- Novel endoscopic posterior fossa cyst fenestration via an occipital meningocele defect in neonatal Dandy-Walker malformation: illustrative case.Journal of neurosurgery. Case lessons · 2026Article
- Dandy-Walker syndrome linked to amelia, genu recurvatum, haemangioma, complex congenital heart defects, schizencephaly, and dyslipidaemia: a case report.BMC pediatrics · 2025Article
- Article
- Retinoblastoma in Dandy-Walker Syndrome.Cureus · 2025Article
- Adult-Onset Syringomyelia in Dandy-Walker Malformation Patients: Clinical Insights and Literature Review.Brain sciences · 2025Article
- Unraveling Dandy-Walker Syndrome: A Case Report with Clinical Presentations and Management Insights.International journal of clinical pediatric dentistry · 2025Article
- A Rare Presentation of Dandy-Walker Syndrome with Meningitis Symptoms in a 3-Month-Old Female: A Case Study From Somalia.Pediatric health, medicine and therapeutics · 2025Article
- Cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome: First case reported in Saudi Arabia.Radiology case reports · 2023Article
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Authors and funding
6 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dandy-Walker syndrome (DWS) is a rare congenital malformation characterized by hypoplasia of the cerebellar vermis and its upward rotation and cystic enlargement of the fourth ventricle. The clinical manifestations include psychomotor retardation, ataxia and hydrocephalus. We report a case of 16-year-old female patient in Ali Abad Teaching Hospital who was suffering from unsteady gait, memory deterioration and urinary incontinence. A brain magnetic resonance imaging revealed enlarged cystic posterior fossa, dilated fourth ventricles and upward rotated cerebellar vermis which were indicating DWS. The patient prepared for planned surgical operation and a written informed consent was obtained from her parents for surgery and general anesthesia. A cystoperitoneal (CP) shunt was placed and then the patient transferred to recovery room. After recovery and hospital stay, the patient discharged with improved clinical symptoms.
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