Familial glucocorticoid deficiency due to a novel TXNRD2 variant: expanding the spectrum of a rare genetic cause - Top-Institutions - 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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Top Institutions in Endocrinology

Brief introduction explaining scope and methodology.

  • #1

    Queen Mary University of London
    Queen Mary University of London

    London, United Kingdom

    Key Differentiators

    • Endocrinology
    • Genetics
  • #2

    University of Bern, University Children’s Hospital
    University of Bern, University Children’s Hospital

    Bern, Switzerland

    Key Differentiators

    • Pediatric Endocrinology
    • Diabetology

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