TY  - CHAP
M1  - Book, Section
TI  - Potter Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - A  possible  genetic  disorder  characterized  by  oligohydramnios  secondary  to  renal  diseases  (bilateral  renal  agenesis,  obstructive  uropathy,  autosomal  recessive  polycystic  kidney  disease,  medullary  dysplastic  kidney,  and  renal  hypoplasia).  Clinical  features  include  Potter  facies  (flattened  nose,  recessed  chin),  pulmonary  hypoplasia,  skeletal  anomalies,  and  congenital  heart  defects.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164082191
ER  -