Literature DB >> 18462928

[Multicystic dysplastic kidney disease: update and information for parents at the time of prenatal diagnosis].

J Bacchetta1, A Liutkus, H Dodat, P Cochat.   

Abstract

Multicystic kidney disease (MCKD) is the most common form of Congenital Abnormality of Kidney and Urinary Tract (CAKUT). This anomaly of renal development is characterized by unilateral enlarged cystic formations and fibrous dysplastic parenchyma. The long-term prognosis is usually good; however because of reduced nephron mass, an early prevention of cardiovascular risk and nephrotoxicity is recommended. A lifelong follow-up of blood pressure, serum creatinine and microalbuminuria seems logical as well as in other patients with a single kidney. MCKD is usually diagnosed during pregnancy so that parents often question about long-term prognosis and follow-up. Therefore, we propose an information sheet for parents.

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Year:  2008        PMID: 18462928     DOI: 10.1016/j.arcped.2008.02.021

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  2 in total

1.  Proximal ureteral atresia, a rare congenital anomaly-incidental finding: a case report.

Authors:  Cosimo Bleve; Maria Luisa Conighi; Lorella Fasoli; Valeria Bucci; Francesco Battaglino; Salvatore Fabio Chiarenza
Journal:  Transl Pediatr       Date:  2017-01

2.  [Prenatal diagnosis of multicystic dysplastic kidney: about 18 cases].

Authors:  Hekmat Chaara; Hind Adadi; Imane Attar; Sofia Jayi; Fatima-Zahra Fdili Alaoui; Moulay Abdelilah Melhouf
Journal:  Pan Afr Med J       Date:  2019-07-31
  2 in total

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