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Prenatal Diagnosis of Autosomal Recessive Polycystic Kidney Disease (ARPKD): Molecular Genetics, Clinical Experience, and Fetal Morphology

✍ Scribed by Zerres, K.; Mucher, G.; Becker, J.; Steinkamm, C.; Rudnik-Schnewborn, S.; Heikkil, P.; Rapola, J.; Salonen, R.; Germino, G.G.; Onuchic, L.; Somlo, S.; Avner, E.D.; Harman, L.A.; Stockwin, J.M.; Guay-Woodford, L.M.

Book ID
122340044
Publisher
Lippincott Williams and Wilkins
Year
1999
Tongue
English
Weight
214 KB
Volume
161
Category
Article
ISSN
0022-5347

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Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology
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Autosomal recessive polycystic kidney disease (ARPKD) is one of the most common hereditary renal cystic diseases and has a high infant mortality. Prenatal diagnosis using fetal sonography can be unreliable, especially in early pregnancy. The ARPKD locus has been mapped to proximal chromosome 6p allo

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## Communicated by Jurgen Horst Autosomal recessive polycystic kidney disease (ARPKD) is one of the most common hereditary renal cystic diseases in children. The clinical spectrum ranges from stillbirth and neonatal demise to survival into adulthood. In a given family, however, patients usually di