Condition: Midfrontal capillary hemangioma


rs1562846694 in ACTL6B;TFR2 gene and Midfrontal capillary hemangioma PMID 31134736 2019 Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination.