# Unraveling Dandy‐Walker Malformation: A Comprehensive Literature Review and Case Insight

**Authors:** Mohammad Bdair, Fathi Milhem, Zaid Sawaftah, Husam Hamshary, Hamza A. Abdul‐Hafez, Moath Hattab, Noor Nabresi, Omar Naseef

PMC · DOI: 10.1002/ccr3.70356 · Clinical Case Reports · 2025-03-24

## TL;DR

This paper reviews Dandy-Walker spectrum disorder and presents a case study emphasizing early diagnosis and multidisciplinary care for better outcomes.

## Contribution

The paper provides a detailed case report and emphasizes the role of early intervention and multidisciplinary management in Dandy-Walker spectrum disorder.

## Key findings

- Early comprehensive imaging and CSF diversion via shunting improved outcomes in a 5-month-old with Dandy-Walker spectrum disorder.
- Multidisciplinary follow-up, including genetic counseling, is crucial for managing developmental and neurological needs in affected children.
- Hydrocephalus-oriented management remains central, but early intervention significantly impacts long-term quality of life.

## Abstract

Dandy‐Walker spectrum disorder (DWSD) is a congenital abnormality of the brain, consisting typically of partial or complete hypoplasia of the cerebellar vermis, cystic dilation of the fourth ventricle, and enlargement of the posterior fossa. Approximately 1 in 10,000 to 30,000 live births is affected by this typically early‐onset neurological condition, which commonly presents with hydrocephalus, irritability, and poor motor coordination. Usually, the diagnosis is confirmed by anatomic features typical of computed tomography or magnetic resonance imaging (MRI). Management has been largely hydrocephalus‐oriented, usually by VP shunting and multidisciplinary follow‐up for neurological and developmental improvement in the long run. Herein is reported a case with a 5‐month‐old male presenting with DWSD, which has been documented in this paper along with his clinical presentation, imaging findings, and, most importantly, the response to the cerebrospinal fluid (CSF) diversion following the shunt. This case highlights the importance of early intervention, early comprehensive imaging, and a multidisciplinary approach, including genetic counseling, in optimizing the quality of life and managing complex developmental needs associated with DWSD.

## Linked entities

- **Diseases:** hydrocephalus (MONDO:0001150)

## Full-text entities

- **Diseases:** congenital abnormality of the brain (MESH:D000013), ventricle (MESH:D002551), hypoplasia of the cerebellar vermis (MESH:C537206), cystic dilation of the (MESH:D018297), neurological condition (MESH:D019636), irritability (MESH:D001523), DWSD (MESH:D003616), hydrocephalus (MESH:D006849)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11932802/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC11932802/full.md

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Source: https://tomesphere.com/paper/PMC11932802