What is Cohen Syndrome? Cohen syndrome is a rare genetic disorder that affects multiple systems in the body. It is caused by mutations in the VPS13B gene, which plays a key role in cellular processes. Though symptoms and severity vary from person to person, some of the most common characteristics include: • Developmental Delays: Children with Cohen syndrome often experience delays in speech, motor skills, and learning. • Vision Problems: Progressive vision loss, including nearsightedness and retinal degeneration, is common. • Low Muscle Tone (Hypotonia): Many children have reduced muscle...
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