Research progress on monogenic inherited glomerular diseases with central nervous system symptoms
CSTR:
Author:
Affiliation:

1.Department of Pediatrics, Third Xiangya Hospital, Central South University, Changsha 410013, China

Clc Number:

Fund Project:

  • Article
  • |
  • Figures
  • |
  • Metrics
  • |
  • Reference
  • |
  • Related
  • |
  • Cited by
  • |
  • Materials
  • |
  • Comments
    Abstract:

    To date, approximately 500 monogenic inherited kidney diseases have been reported, with more than 50 genes associated with the pathogenesis of monogenic isolated or syndromic nephrotic syndrome. Most of these genes are expressed in podocytes of the glomerulus. Neurological symptoms are common extrarenal manifestations of syndromic nephrotic syndrome, and various studies have found connections between podocytes and neurons in terms of morphology and function. This review summarizes the genetic and clinical characteristics of monogenic inherited diseases with concomitant glomerular and central nervous system lesions, aiming to enhance clinicians' understanding of such diseases, recognize the importance of genetic diagnostic techniques for comorbidity screening, and reduce the rates of missed diagnosis and misdiagnosis.

    Reference
    Related
    Cited by
Get Citation

王英,何庆南.伴中枢神经系统症状的单基因遗传性肾小球疾病的研究进展[J].中国当代儿科杂志英文版,2024,(6):652-658

Copy
Share
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:December 12,2023
  • Revised:
  • Adopted:
  • Online: January 14,2025
  • Published:
Article QR Code