Kallmann's syndrome.

dc.contributor.authorKulkarni, M Len_US
dc.contributor.authorBalaji, M Den_US
dc.contributor.authorKulkarni, Akhil Men_US
dc.contributor.authorSushanth, Sen_US
dc.contributor.authorKulkarni, Bhagyavathi Men_US
dc.date.accessioned2007-12-05en_US
dc.date.accessioned2009-05-30T11:27:27Z
dc.date.available2007-12-05en_US
dc.date.available2009-05-30T11:27:27Z
dc.date.issued2007-12-05en_US
dc.description.abstractKallmann's syndrome is a rare genetic disorder due to abnormal migration of olfactory axons and gonadotropin releasing hormone producing neurons, characterized by hypogonadism and anosmia. The prevalence of Kallmann's syndrome is 1:10,000 to 1:60,000 with a male to female ratio of 5:1. The inheritance of Kallmann's syndrome may be X-linked, autosomal recessive or autosomal dominant with variable penetrance, mutation involving KAL-1 and KAL-2 gene respectively. We report a case of Kallmann's syndrome in a 19-year-old boy with characteristic clinical, biochemical and MRI findings.en_US
dc.description.affiliationDepartment of Pediatrics, J.J.M. Medical College, Davangere, Karnataka, India.en_US
dc.identifier.citationKulkarni ML, Balaji MD, Kulkarni AM, Sushanth S, Kulkarni BM. Kallmann's syndrome. Indian Journal of Pediatrics. 2007 Dec; 74(12): 1113-5en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/79694
dc.language.isoengen_US
dc.source.urihttps://medind.nic.in/icb/icbai.shtmlen_US
dc.subject.meshAdulten_US
dc.subject.meshDose-Response Relationship, Drugen_US
dc.subject.meshDrug Administration Scheduleen_US
dc.subject.meshFollow-Up Studiesen_US
dc.subject.meshHumansen_US
dc.subject.meshKallmann Syndrome --diagnosisen_US
dc.subject.meshMaleen_US
dc.subject.meshSeverity of Illness Indexen_US
dc.subject.meshTestosterone --therapeutic useen_US
dc.titleKallmann's syndrome.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
Files
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.79 KB
Format:
Plain Text
Description: