Introduction Kallmann syndrome (KS) is a neuronal migration disorder characterised by hypogonadotropic hypogonadism associated with anosmia or hyposmia. It affects males more than females with a male to female ratio of around 6:11. We report a rare case of Kallmann syndrome with delayed puberty, anosmia and characteristic magnetic resonance imaging (MRI) findings.
How to Cite:
Roy, K. and Das, D., 2016. Kallmann syndrome with characteristic magnetic resonance imaging findings. Sri Lanka Journal of Child Health, 45(4), pp.288–290. DOI: http://doi.org/10.4038/sljch.v45i4.8038