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cerebral palsy / Guillain Barre syndrome/ muscular dystrophy/ Meningomyelocele/ Spina bifida. NEUROMUSCULAR dysfunction. Cerebral palsy? Guillain Barre syndrome? muscular dystrophy?Meningomyelocele? Spina bifida? Neuromuscular dysfunction. Spina bifida is a birth defect where the spine and spinal cord don't close properly in the womb, damaging nerves and potentially causing paralysis, bowel/bladder issues, or hydrocephalus (fluid on the brain). It's caused by genetic and environmental factors, with low maternal folic acid being a major risk factor. Types range from mild (spina bifida occulta, often unnoticed) to severe (myelomeningocele, where a sac with spinal cord protrudes). Guillain-Barré syndrome (GBS) is a rare autoimmune disorder where the immune system attacks the peripheral nerves, causing tingling, weakness, and paralysis that often starts in the legs and spreads upward, potentially affecting breathing muscles. Triggered by infections like Campylobacter or viruses, it requires rapid treatment (like plasma exchange or IVIG) in a hospital, as severe cases are life-threatening but most people recover fully over weeks to years.Muscular Dystrophy (MD) is a group of over 30 genetic disorders causing progressive muscle weakness and wasting, resulting from gene mutations affecting muscle proteins, leading to loss of muscle fibers and function, impacting movement, breathing, and heart function over time, with symptoms varying by type but often including difficulty walking, falling, and eventual need for wheelchairs, managed with treatments that slow progression and manage complications. Key types include Duchenne (DMD) and Becker MD, often starting in childhood, while others emerge in adulthood, and management focuses on physical therapy, supportive care, and sometimes medications. 📝 DISORDER COVERED Muscular dystrophy Guillain Barre syndrome Meningomyelocele Cerebral palsy Spina bifida