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.

Deshmukh, A. and Joshi, R. (0AD) ‘A rare case of Kallmann syndrome with bimanual synkinesis’, Sri Lanka Journal of Medicine, {volume}({issue}), p. {page}. Available at: https://doi.org/10.4038/sljm.v30i1.279.

Deshmukh, Aand R Joshi. “A rare case of Kallmann syndrome with bimanual synkinesis”. Sri Lanka Journal of Medicine, vol. {volume}, no. {issue}, 0AD, p. {page}, doi:10.4038/sljm.v30i1.279.

Deshmukh, A., &amp; Joshi, R. (0AD). A rare case of Kallmann syndrome with bimanual synkinesis. Sri Lanka Journal of Medicine, {volume}({issue}), {page}. https://doi.org/10.4038/sljm.v30i1.279

Deshmukh, A., and R. Joshi. 0AD. “A Rare Case of Kallmann Syndrome with Bimanual Synkinesis”. Sri Lanka Journal of Medicine {volume} ({issue}): {page}. https://doi.org/10.4038/sljm.v30i1.279.

1. Deshmukh A, Joshi R. A rare case of Kallmann syndrome with bimanual synkinesis. Sri Lanka Journal of Medicine. 0AD;{volume}({issue}):{page}. DOI: https://doi.org/10.4038/sljm.v30i1.279

1. Deshmukh A, Joshi R. A rare case of Kallmann syndrome with bimanual synkinesis. Sri Lanka Journal of Medicine. 0AD;{volume}({issue}):{page}. doi:10.4038/sljm.v30i1.279

Deshmukh A and Joshi R, ‘A Rare Case of Kallmann Syndrome with Bimanual Synkinesis’ (0AD) {volume} Sri Lanka Journal of Medicine {page} DOI: https://doi.org/10.4038/sljm.v30i1.279

[1]A. Deshmukh and R. Joshi, “A rare case of Kallmann syndrome with bimanual synkinesis”, Sri Lanka Journal of Medicine, vol. {volume}, no. {issue}, p. {page}, 0AD, doi: 10.4038/sljm.v30i1.279.

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Case Reports

A rare case of Kallmann syndrome with bimanual synkinesis

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