Unilateral form of polycystic kidney disease

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Unilateral and segmental localised polycystic kidney disease.

Unilateral and segmental localised polycystic disease is a rare type of cystic disease of the kidney. It takes the form of a segmental cystic abnormality in one kidney morphologically identical to the autosomal dominant adult form of polycystic kidney disease. The clinical, radiological, and pathological appearances of a case are described. The differential diagnosis and a possible pathogenic m...

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Genetic Diagnosis of a Lethal Form of Autosomal Recessive Polycystic Kidney Disease

Background Autosomal recessive polycystic kidney disease (ARPKD; OMIM number 263200) is a severe early onset hereditary form of polycystic kidney and liver disease. Case Report In the current study, we present a consanguineous couple with a history of an affected son with polycystic kidney disease (PKD), hepatic failure and epileptic seizures who died at the age of 8 months. Both parents were h...

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unilateral enlargement of kidney: a rare manifestation of autosomal recessive polycystic kidney disease

case presentation a preterm neonate with suspicious rt renal mass and oligohydramnios at prenatal ultrasound was hospitalized due to respiratory distress and hypertension. although postnatal ultrasound showed enlarged echogenic rt kidney and normal sized echogenic lt kidney, regarding to linear array transducer findings, arpkd was considered rather than renal mass. the diagnosis was confirmed a...

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Polycystic kidney disease with unilateral ventriculomegaly: a case report

Polycystic Kidney Disease (PKD) is an autosomal recessive disease with an incidence of about 1 in 30,000 births. It characterized by multiple cysts which filled by fluid that can ultimately impede kidney function leading to degeneration of renal tissue and renal failure. Oligo or anhydramnios is frequently present but not invariably so, suggesting that some degree of renal function is retained ...

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Autosomal dominant polycystic kidney disease with ectopic unilateral multicystic dysplastic kidney

BACKGROUND Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disorder. In most cases, ADPKD similarly affects bilateral kidneys. CASE PRESENTATION Among the 605 ADPKD patients that were followed up by our center, we identified two male patients with unilateral ADPKD. The cases were remarkable because the patients also had ectopia and multicystic dysplasi...

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ژورنال

عنوان ژورنال: Nephrology Dialysis Transplantation

سال: 1999

ISSN: 1460-2385,0931-0509

DOI: 10.1093/ndt/14.11.2775-a