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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Meier-Gorlin syndrome

Fig. 1

Facial features of Meier-Gorlin syndrome. Patient A is a girl aged 7 years and 9 months with two mutations in ORC4. Patient B is a 14 year old girl, who carries one mutation in ORC1. Both show the characteristic facial features of MGS, including microtia, a prominent nose with a convex nasal profile, a small mouth with full lips, and retro-/micrognathia

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