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Fig. 3 | BMC Medical Genomics

Fig. 3

From: Novel compound heterozygous variants of the SEC23A gene in a Chinese family with cranio-lenticulo-sutural dysplasia based on data from a large cohort of congenital cataract patients

Fig. 3

The ocular and craniofacial features of a CLSD patient. Bilateral total cataracts and normal macular (A to D). OCT revealed that the central fovea structure of the macular was clearly visible. Besides, the thickness of each layer was within the normal limits. Frontal bossing, wide and delayed closure of the anterior fontanelle, sparse and coarse hair, and pectus excavatum (E and F)

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BMC Medical Genomics

ISSN: 1755-8794

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