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Fig. 1 | Italian Journal of Pediatrics

Fig. 1

From: Intestinal malrotation in a female newborn affected by Osteopathia Striata with Cranial Sclerosis due to a de novo heterozygous nonsense mutation of the AMER1 gene

Fig. 1

a Patient’s front view: frontal bossing, narrow bitemporal diameter, low anterior hairline, facial asymmetry due to left hypoplasia, hypertelorism, epicanthal folds, palpebral ptosis of the left eye, horizontal palpebral fissures, prominent nose, long philtrum and thin lips. b Lateral view: parietal bossing, dysplastic, low-set and posteriorly rotated ear, microretrognathia

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