Successful management of a rare case of double myelomeningocele in an infant: A case report from Pakistan and brief review of pathophysiology

Document Type

Case Report

Department

Surgery; Neurosurgery

Abstract

Neural tube defects (NTDs) are common congenital anomalies, with myelomeningocele (MMC) being the most severe form. Double-level MMC is exceedingly rare, with fewer than 60 cases reported worldwide and none from Southeast Asia. We report a 4-month-old male with two congenital swellings on his back, diagnosed as double MMC at the cervical and lumbar levels, along with hydrocephalus and Arnold–Chiari malformation. Surgical management, including ventriculoperitoneal shunting and MMC repair, resulted in good outcomes. This case highlights the importance of early diagnosis, timely surgical intervention, and prenatal folic acid supplementation to reduce NTD risk in resource-limited settings.

AKU Student

no

Publication (Name of Journal)

Asian Journal of Neurosurgery

DOI

10.1055/s-0045-1811607

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