RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164082191
T1 Potter Syndrome
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=1164082191
RD 2024/04/18
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.