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We have experienced a case of Potter syndrome type I in a newborn infant who presented with severe
respiratory distress soon after birth. The diagnosis was made with autopsy findings consisted of bilateral
polycystic renal dysplasia, bilateral hypoplastic lung , facies renalis, fibrocystic change of liver, patent ductus arteriosus, patent foramen ovale, ureter and urinary bladder hypoplasia and calcaneovarus.
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