TY - JOUR
T1 - Oligohydramnion, renal failure and no pulmonary hypoplasia in glomerulocystic kidney disease
AU - Landau, Daniel
AU - Shalev, Hanna
AU - Shulman, Hanna
AU - Barki, Yehiel
AU - Maor, Esther
AU - Zmora, Ehud
PY - 2000/4
Y1 - 2000/4
N2 - Two newborns with glomerulocystic kidney disease manifesting as late onset oligohydramnion and neonatal anuria, yet without severe respiratory distress, are presented. They had a similar perinatal course and associated clinical manifestations. No associated congenital or inherited malformation syndrome could be defined. Both infants' parents were first degree cousins and belonged to the same small Bedouin tribe, and neither they nor the infants' siblings had polycystic kidneys or renal insufficiency, pointing to either a possible genetic etiology or a common external toxic exposure.
AB - Two newborns with glomerulocystic kidney disease manifesting as late onset oligohydramnion and neonatal anuria, yet without severe respiratory distress, are presented. They had a similar perinatal course and associated clinical manifestations. No associated congenital or inherited malformation syndrome could be defined. Both infants' parents were first degree cousins and belonged to the same small Bedouin tribe, and neither they nor the infants' siblings had polycystic kidneys or renal insufficiency, pointing to either a possible genetic etiology or a common external toxic exposure.
KW - Genetics
KW - Glomerulocystic kidney disease
KW - Oligohydramnion
KW - Renal failure-neonate
UR - https://www.scopus.com/pages/publications/0034073529
U2 - 10.1007/s004670050767
DO - 10.1007/s004670050767
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C2 - 10775077
AN - SCOPUS:0034073529
SN - 0931-041X
VL - 14
SP - 319
EP - 321
JO - Pediatric Nephrology
JF - Pediatric Nephrology
IS - 4
ER -
