Abstract：
:We report a case of autosomal recessive polycystic kidney disease (ARPKD). A presumptive diagnosis was made after a late-term prenatal ultrasound revealed hypoplastic lungs, massive polycystic kidneys, and oligohydramnios. A full-term baby girl was delivered vaginally. Respiratory distress required intubation. Twelve hours after birth, she underwent bilateral nephrectomy and peritoneal dialysis catheter placement. The average kidney size was 150 g and 9.25 cm. Pathologic examination confirmed ARPKD. Peritoneal dialysis was started on the third day of life. The baby had no gross neurologic deficit. At 6 months of age, she was growing well, and the mother was a candidate to be a living-related kidney donor.
journal_name
Urologyjournal_title
Urologyauthors
Munding M,Al-Uzri A,Gralnek D,Riden Ddoi
10.1016/s0090-4295(99)00362-3subject
Has Abstractpub_date
1999-12-01 00:00:00pages
1097issue
6eissn
0090-4295issn
1527-9995pii
S0090-4295(99)00362-3journal_volume
54pub_type
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