Related Experiment Video
Updated: May 15, 2026

Induction of Experimental Autoimmune Hypophysitis in SJL Mice
Published on: December 17, 2010
GLI2 mutations as a cause of hypopituitarism
1Boston Children's Hospital Division of Endocrinology, 300 Longwood Avenue, Boston, MA 02115, USA. laurie.cohen@childrens.harvard.edu
Abstract:
The sonic hedgehog (Shh) signaling pathway is important in pituitary and craniofacial development. Gli2 is a transcription factor that mediates Shh signaling. Mutations in GLI2 have been found in association with holoprosencephaly (HPE) and HPE-like phenotype, with and without pituitary hormone deficiencies; as well as in patients with pituitary dysfunction with and without HPE craniofacial features. Polydactyly is a common associated finding.
Related Concept Videos
Hypothyroidism II: Pathophysiology
Hyperthyroidism II: Pathophysiology
Graves Disease II: Pathophysiology
Cushing Syndrome II: Pathophysiology
Graves' Disease I: Introduction
Hyperthyroidism I: Introduction

