CHINATOWN DIALYSIS CENTER
213 HESTER STREET, 2ND FLR
NEW YORK, NY 10013
(212) 925 - 0404
UPPER EAST SIDE DIALYSIS CENTER
210 EAST 86TH ST, 3RD FLR
NEW YORK, NY 10128
(212) 794-2850
Note: If you are a traveling dialysis patient looking for treatment while visiting the Manhattan/New York City area, you may contact either of the 2 dialysis centers I'm affiliated with, or visit www.dialysisfinder.com
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CAUSES OF END STAGE RENAL DISEASE (ESRD)
DIABETES
type 2, adult-onset type or unspecified type diabetes
type 1, juvenile type, ketosis prone diabetes
GLOMERULONEPHRITIS
glomerulonephritis (GN)
focal glomerulosclerosis, focal sclerosing GN
membranous nephropathy
membranoproliferative GN type 1, diffuse MPGN
dense deposit disease, MPGN type 2
IgA nephropathy, Berger´s disease
IgM nephropathy (proven by immunofluorescence)
rapidly progressive GN
Goodpasture´s Syndrome
post infectious GN, SBE
other proliferative GN
SECONDARY GN/VASCULITIS
lupus erythematosus, (SLE nephritis)
Henoch-Schonlein syndrome
scleroderma
hemolytic uremic syndrome
polyarteritis
Wegener´s granulomatosis
nephropathy due to heroin abuse and related drugs
vasculitis and its derivatives
secondary GN, other
urinary tract tumor (unspecified)
INTERSTITIAL NEPHRITIS/PYELONEPHRITIS
analgesic abuse
radiation nephritis
lead nephropathy
nephropathy caused by other agents
gouty nephropathy
nephrolithiasis
acquired obstructive uropathy
chronic pyelonephritis, reflux nephropathy
chronic interstitial nephritis
acute interstitial nephritis
urolithiasis
nephrocalcinosis
HYPERTENSION/LARGE VESSEL DISEASE
renal disease due to hypertension
renal artery stenosis
renal artery occlusion
cholesterol emboli, renal emboli
CYSTIC/HEREDITARY/CONGENITAL DISEASES
polycystic kidneys, adult type (dominant)
polycystic, infantile (recessive)
medullary cystic disease, including nephronophthisis
tuberous sclerosis
hereditary nephritis, Alport´s syndrome
cystinosis
primary oxalosis
Fabry´s disease
congenital nephrotic syndrome
Drash syndrome, mesangial sclerosis
congenital obstructive uropathy
renal hypoplasia, dysplasia, oligonephronia
prune belly syndrome
hereditary/familial nephropathy
NEOPLASMS/TUMORS
renal tumor (malignant)
urinary tract tumor (malignant)
renal tumor (benign)
urinary tract tumor (benign)
renal tumor (unspecified)
lymphoma of kidneys
multiple myeloma
light chain nephropathy
amyloidosis
complication post bone marrow or other transplant
MISCELLANEOUS CONDITIONS
sickle cell disease/anemia
sickle cell trait and other sickle cell (HbS/Hb other)
post partum renal failure
AIDS nephropathy
traumatic or surgical loss of kidney(s)
hepatorenal syndrome
tubular necrosis (no recovery)
other renal disorders
etiology uncertain
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