GNAO1 mutation-related severe involuntary movements treated with gabapentin

Mutations in GNAO1 typically result in neurodevelopmental disorders, including involuntary movements. They may be improved using calcium-channel modulators.

Source: Brain and Development - December 22, 2020 Category: Neurology Authors: Manami Akasaka, Atsushi Kamei, Sachiko Tanifuji, Maya Asami, Jun Ito, Kanako Mizuma, Kotaro Oyama, Tomoharu Tokutomi, Kayono Yamamoto, Akimune Fukushima, Toshiki Takenouchi, Tomoko Uehara, Hisato Suzuki, Kenjiro Kosaki Tags: Case Report Source Type: research