HIGHLIGHTS
- What: Alport syndrome is a genetically heterogenous disorder resulting from variants in genes coding for alpha-3/4/5 chains of Collagen IV which results in defective basement membranes in the kidney, cochlea and eye.
- Who: Dermot Michael Wildes from the RCSI University of Medicine and Health Sciences, StStephen`s Green, Dublin, Ireland have published the research: An unusual case of nephrotic syndrome, in the Journal: (JOURNAL)
SUMMARY
Case A 15-year-old female presented with a 2-week history of pedal oedema. The following laboratory investigations were performed: Complete blood . . .
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