Una mutación sin sentido homocigota en el gen del receptor de insulina en bebés con leprechaunismo
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Updated: Oct 8, 2026

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
A Krook1, L Brueton, S O'Rahilly
1Department of Medicine, University of Cambridge, Addenbrookes Hospital, UK.
Lancet (London, England)
|July 31, 1993
Resumen
Un recién nacido con resistencia severa a la insulina carecía de receptores de insulina funcionales debido a una mutación genética. Este hallazgo desafía la creencia de que la ausencia completa de receptores de insulina es incompatible con el desarrollo fetal.
Área de la Ciencia:
- Genética La genética.
- Endocrinología Endocrinología.
- Biología del desarrollo Biología del desarrollo.
Sus antecedentes:
- Las mutaciones en el gen del receptor de insulina están relacionadas con la resistencia severa a la insulina.
- La ausencia completa de receptores de insulina no ha sido documentada previamente.
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