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In contrast to FSHD2 individuals, BAMS patients show no signs of muscular dystrophy while SMCHD1 mutations in FSHD2 are not associated with craniofacial defects, which are characteristic for BAMS

I also had food allergies, autoimmune disease, fibromyalgia pain, nerve, joint and muscle pain, recurring Epstein Barr virus and chronically infected tonsils and adenoids, which I subsequently had removed

This effect was largely prevented by inhibitors of de novo ceramide synthesis suggesting the role for ceramide[163]

Richard-Carpentier G, Jabbour E, Short NJ, Rausch CR, Savoy JM, Bose P, Yilmaz M, Jain N, Borthakur G , Ohanian M, Alvarado Y, Rytting M, Kebriaei P, Konopleva M, Kantarjian H, Ravandi F

10.1016/j.bcp.2004.04.003 45 KimJ.AhnC