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DOI: 10.4103/1947-489X.210237
Kallmann syndrome with short stature and pituitary hypoplasia

Kallmann syndrome (KS) is a rare disease in which hypogonadotropic hypogonadism and anosmia co-exist. In KS, the gonadotropic deficiency is isolated, the other pituitary hormones, especially the growth hormone, are preserved. We report the case of a 17 year old male having a sporadic case of KS associated with growth retardation. The diagnosis was based on hormonal workup and specific features on the MRI. The pituitary gland was hypoplastic. The patient was diagnosed to have Kallmann's syndrome with short stature associated to pituitary hypoplasia. To the best of our knowledge, this is the first case to be described in the literature combining KS, short stature and hypoplastic pituitary gland.
Publication History
Received: 05 September 2016
Accepted: 23 September 2016
Article published online:
07 July 2022
© 2016. The Libyan Authority of Scientific Research and Technologyand the Libyan Biotechnology Research Center. All rights reserved. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License,permitting copying and reproductionso long as the original work is given appropriate credit. Contents may not be used for commercial purposes, oradapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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