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Fig. 1 | BMC Medical Genetics

Fig. 1

From: Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature

Fig. 1

The characteristic facies of 2 individuals with DYRK1A mutation. a-b Patient 1 with bitemporal narrowing, down-slanted palpebral fissures, deep-set eyes and dysplastic ears. c MR Images in Patient 1 showing thin corpus callosum, enlarged cisterna magna and 4th ventricle. d distal contractures seen in Patient 1. e-g Patient 2 with with bitemporal narrowing, deep-set eyes and dysplastic ears

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