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Figure 1. . Facial features of individuals with SATB2-associated syndrome caused by intragenic pathogenic variants in SATB2 (A-D), intragenic deletion of SATB2 (E), and large deletions that include SATB2 and other adjacent genes (F-G).

Figure 1.

Facial features of individuals with SATB2-associated syndrome caused by intragenic pathogenic variants in SATB2 (A-D), intragenic deletion of SATB2 (E), and large deletions that include SATB2 and other adjacent genes (F-G). The most consistently reported features include prominent forehead, long face with prominent chin, smooth philtrum, and thin vermilion of the upper lip.

From: SATB2-Associated Syndrome

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Zarate YA, Bosanko K, Fish J. SATB2-Associated Syndrome. 2017 Oct 12 [Updated 2024 Jun 20]. In: Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2024. Figure 1. [Facial features of individuals with...].
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