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Cavum septi pellucidi and cavum Vergae in an infant

Persistent cavum septi pellucidi and cavum Vergae in a 1-month-old boy with severe cerebral hypotonia, seizures, and perisylvian polymicrogyria diagnosed as peroxisomal d-bifunctional protein deficiency. Transverse T1w IR. (Courtesy of Dr. Macaya, University Hospital Vall d'Hebron, Barcelona, Spain.)

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Associated Disorders

  • No disorders are specifically associated with abnormalities of the midline cava. Abnormal development of the midline cava reflects the impact of disorders of cerebral growth and development.