Poretti-Boltshauser Syndrome in a Toddler: Novel Neuroimaging Features and Clinical Presentation

Poretti-Boltshauser syndrome (PBS) is a rare autosomal recessive disorder characterized by cerebellar dysplasia with cysts, developmental delay, and ocular abnormalities. We present a one-year-old male with developmental delay, hypotonia, and abnormal eye movements. Brain magnetic resonance imaging revealed extensive cerebellar dysplasia with multiple cortical and subcortical cysts, an enlarged rhomboid-shaped fourth ventricle, and splayed superior cerebellar peduncles. Genetic testing confirmed compound heterozygous pathogenic variants in the LAMA1 gene, both classified as pathogenic according to American College of Medical Genetics and Genomics (ACMG) guidelines. This case highlights the distinctive neuroimaging pattern of PBS, which can guide early diagnosis and appropriate genetic testing. Recognition of these imaging features is crucial for pediatric radiologists, as early diagnosis enables timely intervention with supportive therapies and genetic counseling for affected families.

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Publication Details

Journal
Cureus
Published
2025-11-20
DOI
https://doi.org/10.7759/cureus.97335
Primary Topic
Genetic Syndromes and Imprinting
Type
article
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article

Poretti-Boltshauser Syndrome in a Toddler: Novel Neuroimaging Features and Clinical Presentation

Nivedita Radder, Shrinivas Radder
Cureus
Genetic Syndromes and Imprinting
article

Poretti-Boltshauser Syndrome in a Toddler: Novel Neuroimaging Features and Clinical Presentation

Nivedita Radder, Shrinivas Radder
article en

Abstract

Poretti-Boltshauser syndrome (PBS) is a rare autosomal recessive disorder characterized by cerebellar dysplasia with cysts, developmental delay, and ocular abnormalities. We present a one-year-old male with developmental delay, hypotonia, and abnormal eye movements. Brain magnetic resonance imaging revealed extensive cerebellar dysplasia with multiple cortical and subcortical cysts, an enlarged rhomboid-shaped fourth ventricle, and splayed superior cerebellar peduncles. Genetic testing confirmed compound heterozygous pathogenic variants in the LAMA1 gene, both classified as pathogenic according to American College of Medical Genetics and Genomics (ACMG) guidelines. This case highlights the distinctive neuroimaging pattern of PBS, which can guide early diagnosis and appropriate genetic testing. Recognition of these imaging features is crucial for pediatric radiologists, as early diagnosis enables timely intervention with supportive therapies and genetic counseling for affected families.

CureusVol. 17(11)
Arkansas Children's Hospital (US), University of Arkansas for Medical Sciences (US)
Openalex Percentile: Top 63%
Genetic Syndromes and Imprinting
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