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ENHengel-Maroofian-Schols Syndrome (HEMARS)
Alias:
Neurodevelopmental Disorder with Spasticity, Facial Dysmorphism, and Brain Abnormalities
Hemars
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Hengel-Maroofian-Schols Syndrome, is also known as neurodevelopmental disorder with spasticity, facial dysmorphism, and brain abnormalities. An important gene associated with Hengel-Maroofian-Schols Syndrome is BCAS3 (BCAS3 Microtubule Associated Cell Migration Factor). Affiliated tissues include brain, and related phenotypes are hyperreflexia and global developmental delay
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