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Fig. 1 | Italian Journal of Pediatrics

Fig. 1

From: Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles

Fig. 1

a and b Patient’s front view at birth and age 4 months: high forehead, frontal bossing, round face, hypotelorism, bilateral microphtalmia, convergent strabismus, epicanthal folds, narrow and down slanting palpebral fissures, broad and depressed nasal root, bulbous tip, anteverted nares, prominent columella, long and hypoplastic philtrum, thin lips with “M” shaped mouth. c and d Lateral view at birth and age 4 months: brachicephaly with flattened occiput, cupped, small and low-set left ear with thick helix, microretrognathia

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Italian Journal of Pediatrics

ISSN: 1824-7288

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