[Autosomal recessive polycystic kidney]. / Avtozomno-retsesivna bubrechna polikistoza.
Vutr Boles
; 29(2): 92-5, 1990.
Article
en Bg
| MEDLINE
| ID: mdl-2238628
A case of a 22 years old woman with autosomal-recessive form of kidney polycystosis is presented. The diagnosis was made in early childhood. A combination of renal anomaly and hepatic fibrosis with manifestations of portal hypertension was present. No deviations from the other internal organs were found. At the age of 12 she entered into the stage of chronic renal failure. The last five years she is on dialysis treatment. She had survived several acute bleedings from esophageal varices. The authors are of the opinion that the case is of interest since patients with autosomal-recessive renal polycystosis very rarely reach majority.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Aberraciones Cromosómicas
/
Genes Recesivos
/
Enfermedades Renales Poliquísticas
Tipo de estudio:
Diagnostic_studies
Límite:
Adult
/
Female
/
Humans
Idioma:
Bg
Revista:
Vutr Boles
Año:
1990
Tipo del documento:
Article
Pais de publicación:
Bulgaria