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H-ABC in Children: Understanding the Condition and Planning Therapy Over Time
H-ABC (Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum) is a rare and progressive neurological condition that affects a child’s brain development, movement, and communication. It is caused by mutations in the TUBB4A gene and is classified under leukodystrophies—a group of disorders that impact white matter and myelin in the brain. Because H-ABC is…
