Literature DB >> 11424964

Kallmann's syndrome: clues to clinical diagnosis.

H John1, C Schmid.   

Abstract

Five cases of Kallmann's syndrome are presented, out-patients with microtestes, hypogonadotropic hypogonadism and complete anosmia. The final diagnosis was made only when they were aged between 17 and 26 (mean 21 years), although they had been seen by several physicians before: 3 for cryptorchidism and 3 for absence of spontaneous puberty; 2 had a positive family history, and 4 of the 5 patients or their parents admitted that they were aware of the fact that their sense of smell was completely absent, but they did not mention it spontaneously.

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Year:  2000        PMID: 11424964     DOI: 10.1038/sj.ijir.3900568

Source DB:  PubMed          Journal:  Int J Impot Res        ISSN: 0955-9930            Impact factor:   2.896


  1 in total

1.  Clinical and inheritance profiles of Kallmann syndrome in Jordan.

Authors:  Mousa A Abujbara; Hanan A Hamamy; Nadim S Jarrah; Nadima S Shegem; Kamel M Ajlouni
Journal:  Reprod Health       Date:  2004-10-24       Impact factor: 3.223

  1 in total

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