Open AccessAutosomal recessive polycystic kidney disease: Case report
Author(s) -
Radmila Stevanović,
Sofija Glumac,
Jovanka Trifunovic,
Biljana Medjo,
Tijastasović,
Jasmina Marković-Lipkovski
Publication year - 2009
Publication title -
srpski arhiv za celokupno lekarstvo
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.135
H-Index - 17
eISSN - 2406-0895
pISSN - 0370-8179
DOI - 10.2298/sarh0906288s
Subject(s) - medicine , oligohydramnios , autosomal recessive polycystic kidney disease , autopsy , polycystic disease , respiratory distress , polycystic kidney disease , pediatrics , kidney , disease , pregnancy , nephronophthisis , pathology , gestation , surgery , biochemistry , chemistry , genetics , gene , phenotype , biology
Autosomal recessive polycystic kidney disease is the most common heritable cystic renal disease occurring in infancy and childhood. The clinical spectrum of signs and symptoms of this disease is widely variable ranging from perinatal death to a milder progressive form, which cannot be diagnosed until adolescence.