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ORPHA:93109· ICD-10 Q63.8· Congenital megacalycosis

Визначення(English summary)

Congenital megacalycosis is a rare renal malformation, characterized by non-obstructive dilation of the renal calyces as well as an increased calyceal number (12-20), with a normal renal pelvis, ureter, and bladder. It may be unilateral or bilateral and is usually asymptomatic unless complicated by nephrolithiasis and urinary tract infection.

Поширеність
<1 / 1 000 000
Успадкування
Unknown
Вік початку
All ages