{"id":12058,"date":"2025-03-13T23:24:31","date_gmt":"2025-03-13T22:24:31","guid":{"rendered":"https:\/\/valintermed.com\/?p=12058"},"modified":"2025-03-13T23:24:31","modified_gmt":"2025-03-13T22:24:31","slug":"mielomeningotsele","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/myelomeningotsele\/","title":{"rendered":"Myelomeningocele"},"content":{"rendered":"
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Myelomeningocele is a form of spinal dysraphism that occurs when the neural tube fails to close properly during embryonic development. The disorder is characterized by a protrusion of the spinal cord membranes and contents through a defect in the spine. Myelomeningocele can cause significant neurological impairment, including motor and sensory dysfunction, as well as various problems with bladder and bowel function. The condition is often accompanied by hydrocephalus and requires a multidisciplinary approach to treatment and rehabilitation. The most common form of the disorder occurs at the lumbar or sacral spine and appears as an external sac containing cerebrospinal fluid, membranes, and possibly neural structures.<\/p>\n

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