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Hereditary chronic progressive nephritis in children
Hereditary nephritis, also known as Alports syndrome (AS), is a familial chronic progressive nephritis. The main clinical feature is hematuria, and some cases may present with proteinuria or nephrotic syndrome. It is often accompanied by neurological hearing impairment and progressive renal dysfunction. In the past 10 years, with the rapid development of molecular biology, the research on AS has entered the molecular and genetic levels. Today, the understanding of its inheritance mode, clinical manifestations, and pathological characteristics is relatively clear.
  • Site of disease:

    Kidney, Ear and Eye
  • Infectious :

    Not contagious
  • Frequent population:

    Infants and young children
  • Related symptoms:

    Thrombocytopenia Difficulty breathing Protruding lens Difficulty swallowing Proteinuria
  • Concurrent disease:

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