Fig. 1From: Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case reportFacial aspect of the patient with Xp11.22 microdeletion at the age of 4 years, showing laterally broad eyebrows, epicanthus, a short nose with a broad nasal bridge, a wide mouth with full lips, and uplifted earlobesBack to article page