Author/Authors :
Alehossein, Mehdi Advanced Diagnostic and Interventional Radiology Research Center (ADIR) - Tehran University of Medical Sciences , Pourgholami, Masoud Department of Radiology - Tehran University of Medical Sciences , Kamrani, Kamyar Department of Pediatrics - Tehran University of Medical Sciences , Soltani, Mohammad Department of Radiology - Tehran University of Medical Sciences , Yazdi, Afshin Department of Radiology - Tehran University of Medical Sciences , Salamati, Payman Advanced Diagnostic and Interventional Radiology Research Center (ADIR) - Tehran University of Medical Sciences
Abstract :
Cutis laxa (CL) is a rare congenital and acquired disorder characterized by loose and redundant skin with reduced elasticity. Three types of congenital cutis laxa have been recognized. Other findings are pulmonary emphysema, bronchiectasia, hernia and diverticulosis. We describe a female neonate involved by cutis laxa syndrome and a positive family history. We focus on the radiologic findings of this case such as multiple bladder diverticulosis, GI diverticulosis and very rare accompanying hypertrophic pyloric stenosis (HPS).
