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

Mirjana KocovaVioleta AnastasovskaAleksandar Petlichkovski Henrik 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