Fig. 1From: Mucopolysaccharidosis IIIB and mild skeletal anomalies: coexistence of NAGLU and CYP26B1 missense variations in the same patient in a Chinese familySerial photographs of the patient. a Hypertonia at one month old, b inguinal hernia and c kyphosis at 100 days old. d Skull deformity and e facial asymmetry at 8 months oldBack to article page