Alport’s syndrome

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在2018年3月14日 (三) 09:57所做的修訂版本 (編輯)
Guhjy (對話 | 貢獻)

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當前修訂版本 (2018年3月14日 (三) 09:57) (編輯) (撤銷)
Guhjy (對話 | 貢獻)

 
第1行: 第1行:
*''X-linked'' inheritance (85%) *''X-linked'' inheritance (85%)
-**Genetic defect in @@color(red):''α5 chain of type IV collagen''@@+**Genetic defect in α5 chain of type IV collagen
**Chromosome Xq22–24 **Chromosome Xq22–24
**Mild in female carriers **Mild in female carriers

當前修訂版本

  • X-linked inheritance (85%)
    • Genetic defect in α5 chain of type IV collagen
    • Chromosome Xq22–24
    • Mild in female carriers
  • AR (15%): α3(IV) or α4(IV) collagen (chromosome 2q35–37)
  • AD (rare): α3(IV) or α4(IV) chains
    • AD & AR: Male & females have equal severity
  • Symptoms and signs
    • Hematuria
    • mild proteinuria (<1–2 g/24 h)
      • Sometimes nephrotic syndrome
    • ESRD
    • Sensorineural hearing loss (60%)
      • Early deafness suggest poor prognosis
    • Bilateral anterior lenticonus, retinal flecks, recurrent corneal erosion
    • Rare: mental retardation, leiomyomatosis, platelet defects
    • Pathology
      • EM: Thin GBM → multilamellations surrounding lucent areas that often contain granules of varying density (split basement membrane)
  • Renal transplantation
    • Anti-GBM antibodies directed toward the collagen epitopes absent in their native kidneys, but overt Goodpasture's syndrome is uncommon and graft survival is good