RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164078842 T1 Milroy’s Disease T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164078842 RD 2024/03/29 AB It is a familial primary congenital lymphedema disorder that involves mainly the lower limbs and is present at birth. Other clinical features include recurrent scrotal swelling, intestinal tract protein loss, persistent pulmonary pleural effusion, and hypoproteinemia. The most common presentation of Milroy Disease is bilateral lower extremity lymphedema hat is normally accompanied by hydrocele.