Abstract
Kallmann syndrome is a rare inherited disorder characterized by hypogonadotropic hypogonadism and anosmia or hyposmia. Such cases are mostly diagnosed in adolescent period with complaints of failure to achieve puberty. Early diagnosis and treatment can restore secondary sexual characteristics in such patients. We report a case of a 17-year-old male with Kallmann syndrome who came with hypogonadism and bimanual synkinesis.
DOI: https://doi.org/10.4038/sljm.v30i1.279 | Journal eISSN: 2579-1990
Language: English
Page range: 113 - 116
Published on: Jul 1, 2021
Published by: The Kandy Society of Medicine
In partnership with: Paradigm Publishing Services
Keywords:
© 2021 A. Deshmukh, R. Joshi, published by The Kandy Society of Medicine
This work is licensed under the Creative Commons Attribution 4.0 License.