TY  - CHAP
M1  - Book, Section
TI  - Potter Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - A  possible  genetic  disorder  characterized  by  oligohydramnios  secondary  to  renal  diseases  such  as  bilateral  renal  agenesis.  Other  possible  renal  defects  include  obstructive  uropathy,  autosomal  recessive  polycystic  kidney  disease,  medullary  dysplastic  kidney,  and  renal  hypoplasia.  Clinical  features  include  Potter  facies  (i.e.,  flattened  nose,  recessed  chin),  pulmonary  hypoplasia,  skeletal  anomalies,  and  congenital  heart  defects.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/18
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58083690
ER  -