Oti, Bibiana I. and Okorie, Geoffrey and Chime, Peter and Chime, Ethel and Ezeala-Adikaibe, Birinus and Orjioke, Casmir and Ekochin, Fintan Chinweike and Abonyi, Michael C. (2024) Hypergonadotrophic Hypogonadism with Cerebellar Ataxia in a Twenty-Six-Year-Old Female: A Case Report. Open Journal of Modern Neurosurgery, 14. pp. 83-90.
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Dr Ekochin Article - Case Report GHS.pdf Download (295kB) |
Abstract
Gordon Holmes Syndrome is a rare inherited disease characterized by both neurological and reproductive signs and symptoms. Most patients develop neurologic challenges in early adulthood and cerebellar ataxia occurs as the disease progresses. In the majority of patients, hypogonadism is hypogona dotropic but rarely hypergonadotropic. We report a case of a 26-year-old fe male in Nigeria, with hypergonadotropic hypogonadism and cerebellar atro phy from a non-consanguineous marriage and no family history.
| Item Type: | Article |
|---|---|
| Subjects: | R Medicine > RZ Other systems of medicine |
| Divisions: | Faculty of Medicine, Health and Life Sciences > School of Medicine |
| Depositing User: | mrs chioma hannah |
| Date Deposited: | 02 Jul 2025 11:04 |
| Last Modified: | 02 Jul 2025 11:04 |
| URI: | http://eprints.gouni.edu.ng/id/eprint/4949 |
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