Dandy Walker Malformation Associated with Toxoplasmosis Infection in the Second Trimester: a Case Report

Dandy-Walker Malformation (DWM) is a rare congenital brain disorder affecting the cerebellum and posterior fossa, occurring in 1 in 35,000 births.It is characterized by agenesis of the cerebellar vermis, fourth ventricle dilation, and an enlarged posterior fossa.Genetic factors, chromosomal abnormalities, and infections like rubella, CMV, and toxoplasmosis contribute to its etiology.This case describes a 16-year-old pregnant woman whose fetus was diagnosed with Dandy-Walker malformation (DWM) at 23.3 weeks.Prenatal findings included severe intrauterine growth restriction, absence of the cerebellar vermis, dysgenesis of the corpus callosum, and cardiac abnormalities.PCR confirmed Toxoplasma gondii infection.Despite treatment, fetal death occurred at 24 weeks.Karyotype analysis ruled out chromosomal abnormalities, suggesting a rare infectious etiology rather than a genetic cause.This case highlights the importance of prenatal toxoplasmosis screening, as its early detection can suggest an accurate diagnosis and timely treatment.It also broadens the understanding of DWM beyond its genetic origin, linking it to parasitic infections, in this case, caused by Toxoplasma gondii.josha.org

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Journal
Journal of Science Humanities and Arts - JOSHA
Published
2025-01-01
DOI
https://doi.org/10.17160/josha.12.2.1036
Primary Topic
Fetal and Pediatric Neurological Disorders
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article
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article

Dandy Walker Malformation Associated with Toxoplasmosis Infection in the Second Trimester: a Case Report

German Andres Guevara Lizarazo
Journal of Science Humanities and Arts - JOSHA
Fetal and Pediatric Neurological Disorders
article

Dandy Walker Malformation Associated with Toxoplasmosis Infection in the Second Trimester: a Case Report

German Andres Guevara Lizarazo
article en

Abstract

Dandy-Walker Malformation (DWM) is a rare congenital brain disorder affecting the cerebellum and posterior fossa, occurring in 1 in 35,000 births.It is characterized by agenesis of the cerebellar vermis, fourth ventricle dilation, and an enlarged posterior fossa.Genetic factors, chromosomal abnormalities, and infections like rubella, CMV, and toxoplasmosis contribute to its etiology.This case describes a 16-year-old pregnant woman whose fetus was diagnosed with Dandy-Walker malformation (DWM) at 23.3 weeks.Prenatal findings included severe intrauterine growth restriction, absence of the cerebellar vermis, dysgenesis of the corpus callosum, and cardiac abnormalities.PCR confirmed Toxoplasma gondii infection.Despite treatment, fetal death occurred at 24 weeks.Karyotype analysis ruled out chromosomal abnormalities, suggesting a rare infectious etiology rather than a genetic cause.This case highlights the importance of prenatal toxoplasmosis screening, as its early detection can suggest an accurate diagnosis and timely treatment.It also broadens the understanding of DWM beyond its genetic origin, linking it to parasitic infections, in this case, caused by Toxoplasma gondii.josha.org

Journal of Science Humanities and Arts - JOSHAVol. 12(2)
Universidad Autónoma de Bucaramanga (CO)
Zero hunger
Openalex Percentile: Top 93%
Fetal and Pediatric Neurological Disorders
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Dandy Walker Malformation Associated with Toxoplasmosis Infection in the Second Trimester: a Case Report — German Andres Guevara Lizarazo · Journal of Science Humanities and Arts - JOSHA (2025) | TGRS Research Map | TGRS