Hereditary spherocytosis

Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.

Hydronephrosis

Severe distention of the kidney with dilation of the renal pelvis and calices.


Total: 1

                       


(per page)
PMID (PMCID)
2059799
 FEMALE Adult
Hereditary sacral agenesis with presacral mass and anorectal stenosis: the Currarino triad.
O'Riordain DS, O'Connell PR, Kirwan WO.
Br J Surg. 1991;78(5):536-8.
Other associated abnormalities included tethering of the cord, hydrocephalus, duplex ureter, hydronephrosis, vesicoureteric reflux, neurogenic bladder, bicornuate uterus, rectovaginal fistula and hereditary spherocytosis.