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Figure 1 | Orphanet Journal of Rare Diseases

Figure 1

From: KBG syndrome

Figure 1

Frontal (a) and lateral (b) view of a KBG patient with typical facial dysmorphisms including low frontal hairline, wide eyebrows with mild synophrys, hypertelorism, prominent and high nasal bridge, anteverted nostrils, long philtrum, thin upper lip and prominent anteverted ears. Macrodontia of upper central incisors is observable.

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