Klinik für Kinderheilkunde II - Kindernephrologie am Universitätsklinikum Essen Assigned diseases:
In the following you will find the diseases that are treated in this facility:
Alport syndrome
Atypical hemolytic uremic syndrome
Autosomal dominant polycystic kidney disease
Autosomal recessive polycystic kidney disease
BOR syndrome
Bardet-Biedl syndrome
Bartter syndrome
Beckwith-Wiedemann syndrome
CHARGE syndrome
Congenital and infantile nephrotic syndrome
Cystinuria
Genetic primary hypomagnesemia
Genetic primary hypomagnesemia with hypocalciuria
Genetic primary hypomagnesemia with normocalciuria
Gitelman syndrome
Glomerular disease
Idiopathic steroid-sensitive nephrotic syndrome
Jeune syndrome
Joubert syndrome
Multicystic dysplastic kidney
Nephrogenic diabetes insipidus
Nephronophthisis
Primary glomerular disease
Primary hyperoxaluria
Primary hypomagnesemia with hypercalciuria and nephrocalcinosis
Primary membranoproliferative glomerulonephritis
Renal agenesis
Renal coloboma syndrome
Renal dysplasia
Renal hypoplasia
Renal or urinary tract malformation
Senior-Loken syndrome
Shiga toxin-associated hemolytic uremic syndrome
Thrombotic microangiopathy
Townes-Brocks syndrome