Skip to main content
Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

Fig. 1

Images depicting key phenotypic features of the cases presented here. a Patient 1 facies at 16 years of age, b and c Patient 2 facies at 11 years, d Patient 3 facies at 9 years, e Patient 4 facies at 8 years, and f Patient 5 facies at 6 years. Panels g to k show the patient’s gestalt (at the same age as the facies figure). l Patient 1 hand. m and n Patient 5 ft and hands

Back to article page