Fig. 1From: A novel, putatively null, FGD1 variant leading to Aarskog-Scott syndrome in a family from UAEClinical features of the proband (the elder brother) with Aarskog-Scott syndrome: Panel a illustrates facial dysmorphic features. Panels b and c illustrate skeletal abnormalities in the patient. Panel d shows a pedigree of the affected familyBack to article page