Hypergonadotrophic hypogonadism and cerebellar ataxia in an Indian adolescent: A rare report
- PMID: 26962362
- PMCID: PMC4770668
- DOI: 10.4103/1817-1745.174442
Hypergonadotrophic hypogonadism and cerebellar ataxia in an Indian adolescent: A rare report
Figures
References
-
- Holmes G. A form of familial degeneration of the cerebellum. Brain. 1907;30:466–89.
-
- Seminara SB, Acierno JS, Jr, Abdulwahid NA, Crowley WF, Jr, Margolin DH. Hypogonadotropic hypogonadism and cerebellar ataxia: Detailed phenotypic characterization of a large, extended kindred. J Clin Endocrinol Metab. 2002;87:1607–12. - PubMed
-
- Neuhäuser G, Opitz JM. Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism. Clin Genet. 1975;7:426–34. - PubMed
-
- Amor DJ, Delatycki MB, Gardner RJ, Storey E. New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafness. Am J Med Genet. 2001;99:29–33. - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources