A Rare Presentation of Dandy-Walker Syndrome with Meningitis Symptoms in a 3-Month-Old Female: A Case Study From Somalia

Dandy-Walker Syndrome (DWS) is a rare cerebellar malformation characterized by the underdevelopment of the cerebellar vermis and associated complications. This case report presents a 3-month-old female from Somalia who exhibited fever, loss of consciousness, vomiting, and developmental delays. Neurological examination suggested signs of meningitis, and MRI revealed an enlarged posterior fossa consistent with DWS. Despite initial antibiotic treatment for suspected bacterial meningitis, CSF cultures yielded no growth, raising concerns about prior antibiotic use. Unfortunately, the patient's condition deteriorated, leading to her death. This case highlights the diagnostic challenges of DWS in resource-limited settings and emphasizes the need for improved healthcare access, early diagnosis, and intervention for rare neurological conditions.

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Publication Details

Journal
Pediatric Health Medicine and Therapeutics
Published
2025-03-01
DOI
https://doi.org/10.2147/phmt.s501020
Citations
1
Primary Topic
Fetal and Pediatric Neurological Disorders
Type
article
Field-Weighted Citation Impact
3.49
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article

A Rare Presentation of Dandy-Walker Syndrome with Meningitis Symptoms in a 3-Month-Old Female: A Case Study From Somalia

Mohamoud Hashi Abdi, Abdirahman Omer Ali, H Ahmed, H Ahmed et al.
1 citations
Pediatric Health Medicine and Therapeutics
Fetal and Pediatric Neurological Disorders
3.49
article

A Rare Presentation of Dandy-Walker Syndrome with Meningitis Symptoms in a 3-Month-Old Female: A Case Study From Somalia

Mohamoud Hashi Abdi, Abdirahman Omer Ali, H Ahmed, H Ahmed, Salah Abdikarim Abdilahi, Abdirasak Abdulkadir Muse
article en
1 citations

Abstract

Dandy-Walker Syndrome (DWS) is a rare cerebellar malformation characterized by the underdevelopment of the cerebellar vermis and associated complications. This case report presents a 3-month-old female from Somalia who exhibited fever, loss of consciousness, vomiting, and developmental delays. Neurological examination suggested signs of meningitis, and MRI revealed an enlarged posterior fossa consistent with DWS. Despite initial antibiotic treatment for suspected bacterial meningitis, CSF cultures yielded no growth, raising concerns about prior antibiotic use. Unfortunately, the patient's condition deteriorated, leading to her death. This case highlights the diagnostic challenges of DWS in resource-limited settings and emphasizes the need for improved healthcare access, early diagnosis, and intervention for rare neurological conditions.

Pediatric Health Medicine and TherapeuticsVol. Volume 16
Amoud University (SO), SNUH SMG-SNU Boramae Medical Center (KR)
Gender equality
Openalex Percentile: Top 11%
Fetal and Pediatric Neurological Disorders
3.49
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A Rare Presentation of Dandy-Walker Syndrome with Meningitis Symptoms in a 3-Month-Old Female: A Case Study From Somalia — Mohamoud Hashi Abdi, Abdirahman Omer Ali, et al. · Pediatric Health Medicine and Therapeutics (2025) | TGRS Research Map | TGRS