TY  - CHAP
M1  - Book, Section
TI  - Milroy’s Disease
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
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.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/20
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164078842
ER  -