2007Indian Journal of UrologyOpen access

Autosomal recessive polycystic kidney disease diagnosed in fetus

Joseph Thomas, AP Manjunath, Lavanya Rai, Ranjini Kudva

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Abstract

The presence of isolated large and hyperechoic fetal kidneys suggest polycystic kidney disease. The antenatal diagnosis has to be made without doubt as it has serious implications in the continuation of pregnancy, evaluation of family members and genetic counseling for the family. We present the features of autosomal recessive polycystic kidney disease (ARPKD) diagnosed antenatally by ultrasound and confirmed by fetal autopsy.

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The presence of isolated large and hyperechoic fetal kidneys suggest polycystic kidney disease. The antenatal diagnosis has to be made without doubt as it has serious implications in the continuation of pregnancy, evaluation of family members and genetic counseling for the family. We present the features of autosomal recessive polycystic kidney disease (ARPKD) diagnosed antenatally by ultrasound and confirmed by fetal autopsy.

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Available abstract

The presence of isolated large and hyperechoic fetal kidneys suggest polycystic kidney disease. The antenatal diagnosis has to be made without doubt as it has serious implications in the continuation of pregnancy, evaluation of family members and genetic counseling for the family. We present the features of autosomal recessive polycystic kidney disease (ARPKD) diagnosed antenatally by ultrasound and confirmed by fetal autopsy.

Key concepts: Medicine, Autosomal Recessive Polycystic Kidney Disease, Fetus, Disease, Polycystic disease, Polycystic kidney disease, Autosomal dominant polycystic kidney disease, Kidney

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