A case of congenital Rett variant in a Chinese patient caused by a FOXG1 mutation

Niu, Y; Cao, LR; Zhao, P; Cai, CG

Cao, LR (corresponding author), Tianjin Med Univ, Grad Coll, 22 Qixiang Tai Rd, Tianjin 300070, Peoples R China.

ANNALS OF SAUDI MEDICINE, 2020; 40 (4): 347

Abstract

Rett syndrome (RTT) is a severe progressive neurodevelopmental disease characterized by psychomotor regression. The FOXG1 gene is one of the pathogeni......

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