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First insights into the genetics of 21-hydroxylase deficiency in the Roma population.

Mirjana KocovaVioleta AnastasovskaAleksandar PetlichkovskiHenrik Falhammar
Published in: Clinical endocrinology (2021)
The Roma population in North Macedonia had a very high incidence of classic 21OHD. Almost all patients had the severe salt-wasting form and the In2G/In2G genotype.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • chronic kidney disease
  • newly diagnosed
  • risk factors
  • peritoneal dialysis
  • prognostic factors
  • early onset
  • patient reported outcomes
  • patient reported