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For contributors- A rare genetically confirmed case of apparent mineralocorticoid excess syndrome due to a homozygous HSD11B2 variant in a 2-year-old child with severe hypertension: response to targeted therapy
- Bashair Alabbasi, Mugahid Elamin, Ghadah Alsallum et al.
- Clin Exp Pediatr. 2026;69(8):676-679.