| Acute kidney injury (AKI) |
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Patients with significant renal impairment due to acute illness who requires further assessment
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Patients who require or potentially require acute kidney replacement therapy
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| Chronic kidney disease (CKD) |
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Stage III-V (GFR < 60 ml/min/1.73m²) CKD or
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Any Stage of CKD with other concerns
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| Kidney failure (KF) |
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Stage V CKD (GFR < 15ml/min/1.73m²) requiring long term kidney replacement therapy, including peritoneal dialysis, haemodialysis or transplant
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| Childhood nephrotic syndrome |
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Nephrotic syndrome with atypical features requiring further work up, including kidney biopsy or genetic testing
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Congenital or infantile nephrotic syndrome
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Steroid dependent nephrotic syndrome on second line immunosuppressants
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Steroid resistant nephrotic syndrome
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Any types of nephrotic syndrome with clinical concern, such as renal impairment or systemic manifestations
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| Childhood acute or chronic glomerulonephritis (GN) (including lupus nephritis, vasculitis, IgAN, IgAVN, post-infectious GN or any GN associated with systemic conditions) |
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Any childhood GN which requires further evaluation and management
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| Complement mediated kidney disease or Thrombotic Microangiopathies (TMA) |
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Primary or secondary TMA for evaluation and management
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| Urinary tract infection (UTI) with congenital kidney and urinary tract abnormalities (CAKUT) |
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Patients with significant structural abnormalities of the kidney and urinary tract, including VUR or obstructions
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Patients needing imaging or surgical assessment or evaluation
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| Congenital abnormality of kidney and urinary tract (CAKUT) |
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Patients needing imaging or surgical assessment or evaluation
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| Childhood hypertension or renal vascular diseases |
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Significant hypertension, secondary hypertension, or suspected reno-vascular conditions for evaluation and diagnosis
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| Renal stone disease |
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Paediatric renal stone disease for work up
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Complications secondary to stones disease
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| Genetic kidney diseases (including cystic kidney diseases, hereditary nephropathy and others) |
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Examples include autosomal-dominant polycystic kidney disease (ADPKD), autosomal-recessive polycystic kidney disease (ARPKD), nephronothisis, Alport Syndrome, and other genetic kidney diseases requiring diagnostic evaluation and management
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| Miscellaneous kidney diseases (including metabolic diseases, Tubular disorders, familial kidney diseases, severe fluid or electrolyte disturbances, voiding dysfunction, enuresis related problems, proteinuria, haematuria etc.) |
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Various conditions with kidney involvement requiring focused diagnostic evaluation and management
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