Figure 2From: WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological featuresPicture of the patient at age 2 (a) showing the typical narrow forehead with frontal bossing, hypertelorism with epicanthal folds, up-slanting palpebral fissures, wide depressed nasal bridge, mid macrocephaly. Picture of the patient’s mother at age 3 (b) showing mild hypertelorism with epicanthal folds and a slightly depressed nasal bridge.Back to article page