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Figure 2 | Italian Journal of Pediatrics

Figure 2

From: 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 features

Figure 2

Picture 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.

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Italian Journal of Pediatrics

ISSN: 1824-7288

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