منابع مشابه
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...
متن کاملPolycystic 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 ...
متن کاملunilateral 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...
متن کاملAutosomal 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...
متن کاملPolycystic kidney disease.
A number of inherited disorders result in renal cyst development. The most common form, autosomal dominant polycystic kidney disease (ADPKD), is a disorder most often diagnosed in adults and caused by mutation in PKD1 or PKD2. The PKD1 protein, polycystin-1, is a large receptor-like protein, whereas polycystin-2 is a transient receptor potential channel. The polycystin complex localizes to prim...
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ژورنال
عنوان ژورنال: American Journal of Roentgenology
سال: 1978
ISSN: 0361-803X,1546-3141
DOI: 10.2214/ajr.130.6.1165