Fig. 1From: Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A geneFigures 1a and 1b demonstrate the facial phenotype of the patient. Large head with persistent fontanels, telecanthus, small palpebral fissures, small pinched upturned nose with elfin facies. Figure 1c demonstrates the significant growth restriction at 3 years and 2 months of ageBack to article page