Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report
Author:
Publisher
Baishideng Publishing Group Inc.
Subject
General Medicine
Reference13 articles.
1. Molecular Analysis ofLHX3andPROP-1in Pituitary Hormone Deficiency Patients with Posterior Pituitary Ectopia1
2. A novel mutation of LHX3 is associated with combined pituitary hormone deficiency including ACTH deficiency, sensorineural hearing loss, and short neck—a case report and review of the literature
3. Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss
4. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
5. Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development
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1. A Nonsynonymous Substitution of Lhx3 Leads to Changes in Body Size in Dogs and Mice;Genes;2024-06-04
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