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Blake pouch cyst is a non-syndromic, usually benign, cystic malformation of the posterior fossa characterized by a midline outpouching of the superior medullary velum into the cisterna magna that results from failure of the rudimental fourth ventricular tela choroidea to regress during embryogenesis. Patients can be asymptomatic or present in childhood or adulthood with clinical manifestations of hydrocephalus, such as headache, hypotonia, vertigo, syncope, vomiting, blurred or double vision, nystagmus, papilledema, and delayed gait development.
Biomarker and diagnostic research for Blake pouch cyst has been reported in the published literature.
No clinical trials have been registered for Blake pouch cyst.
4 publications have been identified in PubMed for Blake pouch cyst. Research spans Other (25%), Diagnostic / Biomarker (25%), and Case Report / Case Series (25%).
Pomar L (2025). [PMID: 40325886](https://pubmed.ncbi.nlm.nih.gov/40325886/). *Ultrasound Obstet Gynecol*. [Epidemiology / Natural History]
Makkiyah FA (2025). [PMID: 41036045](https://pubmed.ncbi.nlm.nih.gov/41036045/). *Surg Neurol Int*. [Case Report / Case Series]
Ponmozhi G (2025). [PMID: 40435966](https://pubmed.ncbi.nlm.nih.gov/40435966/). *Fetal Diagn Ther*. [Other]
Guo C (2024). [PMID: 39707235](https://pubmed.ncbi.nlm.nih.gov/39707235/). *BMC Pregnancy Childbirth*. [Diagnostic / Biomarker]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 1:53 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Blake pouch cyst