Literature DB >> 3153307

Genetics of cystic kidney diseases. Criteria for classification and genetic counselling.

K Zerres1.   

Abstract

Despite the high incidence of cystic kidney diseases, affected families are not usually well informed of the inheritance of these disorders. Genetic counselling must be based on precise diagnostic criteria. Detailed information on the different types of cystic kidney disease is summarized, including clinical features, pathology, radiology, prenatal diagnosis and the risk of recurrence. In addition, a genetic interpretation is given of the Caroli syndrome, Potter sequence as well as congenital hepatic fibrosis.

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Year:  1987        PMID: 3153307     DOI: 10.1007/bf00849243

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  34 in total

1.  Bilateral polycystic disease of the kidneys; a follow-up of two hundred and eighty-four patients and their families.

Authors:  O Z DALGAARD
Journal:  Acta Med Scand Suppl       Date:  1957

2.  Bilateral absence of the kidneys and ureters. Three cases reported in one family.

Authors:  H M Pashayan; T Dowd; A V Nigro
Journal:  J Med Genet       Date:  1977-06       Impact factor: 6.318

3.  Polycystic disease of kidney and liver presenting in childhood.

Authors:  H Blyth; B G Ockenden
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

4.  Attitudes to early diagnosis of polycystic kidney disease.

Authors:  K Zerres; M Stephan
Journal:  Lancet       Date:  1986-12-13       Impact factor: 79.321

5.  The nephronophthisis complex. A clinicopathologic study in children.

Authors:  R Waldherr; T Lennert; H P Weber; H J Födisch; K Schärer
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1982

6.  Failure to detect polycystic kidneys in utero by second trimester ultrasonography.

Authors:  J L Simpson; R E Sabbagha; S Elias; C Talbot; R K Tamura
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

7.  The diagnosis of congenital renal anomalies with ultrasound. II. Infantile polycystic kidney disease.

Authors:  R Romero; M Cullen; P Jeanty; P Grannum; E A Reece; I Venus; J C Hobbins
Journal:  Am J Obstet Gynecol       Date:  1984-10-01       Impact factor: 8.661

8.  Genetic counseling in adult polycystic kidney disease.

Authors:  S Sahney; L Weiss; N W Levin
Journal:  Am J Med Genet       Date:  1982-04

9.  A pedigree study of perinatally lethal renal disease.

Authors:  A Bankier; M de Campo; R Newell; J G Rogers; D M Danks
Journal:  J Med Genet       Date:  1985-04       Impact factor: 6.318

10.  Impairment of drug metabolism in polycystic non-parasitic liver disease.

Authors:  E A Sotaniemi; P V Luoma; P M Järvensivu; K A Sotaniemi
Journal:  Br J Clin Pharmacol       Date:  1979-10       Impact factor: 4.335

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  1 in total

Review 1.  Autosomal recessive polycystic kidney disease.

Authors:  K Zerres
Journal:  Clin Investig       Date:  1992-09
  1 in total

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