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Figure 1 | Italian Journal of Pediatrics

Figure 1

From: From hypertransaminasemia to mucopolysaccharidosis IIIA

Figure 1

Dysmorphic features of our patient. Facial dysmorphism (coarse facial features, the slightly depressed nasal bridge, prominent eyebrows, low set ears, malocclusion, full cheeks, wiry and dry hair and the short neck) and skeletal symptoms (genu valga, varus feet, and stocky hands) seen in our patient.

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