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Endocrine Abstracts (2025) 110 EP834 | DOI: 10.1530/endoabs.110.EP834

ECEESPE2025 ePoster Presentations Growth Axis and Syndromes (132 abstracts)

The clinical and mutational spectrum of ulnar-mammary syndrome: two case reports and literature review

Xiaoyan Wang 1


1children’s hospital of soochow university, suzhou, China


JOINT1548

Objective: The aim of this study was to investigate the clinical and genetic characteristics of three cases of short stature caused by the GHSR gene mutation.

Methods: A retrospective analysis was conducted on the clinical data and genetic test results of three cases of short stature caused by the GHSR gene mutation. The patients were followed up at the Department of Endocrinology Genetics and Metabolism of the Children’s Hospital of Soochow University. A literature search (search terms included “GHSR” and “short stature”) for recently published studies was completed using the China National Knowledge Infrastructure database, WanFang database, PubMed, and the Human Gene Mutation Database.ResultsThe peak value of growth hormone provocation test in two cases was >10 ng/ml, and the height of two patients was improved after recombinant human growth hormone therapy. One untreated patient was followed up until lifelong height was reached, and the patient remained with a short stature.

Conclusion: The peak value of growth hormone provocation test in patients with GHSR gene variants may be >10 ng/ml, these patients may have precocious puberty, and short stature caused by the GHSR gene mutation can be treated with growth hormone.

Volume 110

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course

European Society of Endocrinology 
European Society for Paediatric Endocrinology 

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