Literature DB >> 6612920

Infantile polycystic kidney disease: an imaging dilemma.

F B Stapleton, H L Magill, D R Kelly.   

Abstract

Infantile and adult type polycystic kidney diseases are 2 disparate genetic disorders and generally are easily distinguishable on the basis of clinical, pathologic, and radiologic findings. We present 3 children with infantile polycystic kidney disease, ages 9 months to 6 years, in whom the excretory urogram and/or renal ultrasound or gross anatomical appearance of the kidneys resembled adult polycystic kidney disease. The findings from these 3 patients emphasize the importance of renal and liver biopsies in the diagnosis of cystic kidney disease in young children.

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Year:  1983        PMID: 6612920     DOI: 10.1007/bf02926777

Source DB:  PubMed          Journal:  Urol Radiol        ISSN: 0171-1091


  4 in total

1.  Ultrasonographic findings in congenital nephrotic syndrome.

Authors:  V S Bratton; E N Ellis; J T Seibert
Journal:  Pediatr Nephrol       Date:  1990-09       Impact factor: 3.714

2.  Does liver biopsy provide sufficient diagnostic information to differentiate autosomal recessive from autosomal dominant polycystic kidney disease?

Authors:  B R Cole
Journal:  Pediatr Nephrol       Date:  1994-08       Impact factor: 3.714

Review 3.  Sonographically detectable cysts in polycystic kidney disease in newborn and young infants.

Authors:  J L Worthington; G D Shackelford; B R Cole; E D Tack; J M Kissane
Journal:  Pediatr Radiol       Date:  1988

4.  Nephrocalcinosis in a child with autosomal dominant polycystic kidney disease and a prolapsing ectopic ureterocele.

Authors:  E M Burton; J D Hanna; M G Mercado-Deane
Journal:  Pediatr Radiol       Date:  1995
  4 in total

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