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A rare case of Kallmann syndrome with bimanual synkinesis

Authors:

A. Deshmukh ,

Bai Jerbai Wadia children hospital, Mumbai, IN
About A.
Department of Paediatrics
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R. Joshi

Bai Jerbai Wadia children hospital, Mumbai, IN
About R.
Department of Paediatrics
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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.
How to Cite: Deshmukh, A. and Joshi, R., 2021. A rare case of Kallmann syndrome with bimanual synkinesis. Sri Lanka Journal of Medicine, 30(1), pp.113–116. DOI: http://doi.org/10.4038/sljm.v30i1.279
Published on 01 Jul 2021.
Peer Reviewed

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