Familial glucocorticoid deficiency due to a novel TXNRD2 variant: expanding the spectrum of a rare genetic cause - Poll - MDSpire

Familial glucocorticoid deficiency due to a novel TXNRD2 variant: expanding the spectrum of a rare genetic cause

  • By

  • Ibrahim Al Alwan

  • Kheloud M. Alhamoudi

  • Abdullah Ibrahim Alzaben

  • Beshaier Almulhem

  • Nawal Qawasmi

  • Meshael Alswailem

  • Sara Alotaibi

  • Burair Alsaihati

  • Amjad Jabaan

  • Moeber Mahzari

  • Christa E. Flück

  • Ali S. Alzahrani

  • May 28, 2026

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Original Source(s)

Familial glucocorticoid deficiency due to a novel TXNRD2 variant: expanding the spectrum of a rare genetic cause

  • by Ibrahim Al Alwan, Kheloud M. Alhamoudi, Abdullah Ibrahim Alzaben, Beshaier Almulhem, Nawal Qawasmi, Meshael Alswailem, Sara Alotaibi, Burair Alsaihati, Amjad Jabaan, Moeber Mahzari, Christa E. Flück, Ali S. Alzahrani

  • May 28, 2026

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