Fig. 1From: A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case reportFacial appearance at 7 years and 2 months old. Several facial anomalies, such as broad forehead, short philtrum, micrognathia and prominent lobule of the ear, were observed. We obtained permission from the parents to post this photographBack to article page