Familial spastic paraplegia with Kallmann's syndrome.
Open Access
- 1 July 1983
- journal article
- case report
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 46 (7) , 671-674
- https://doi.org/10.1136/jnnp.46.7.671
Abstract
A sibship is reported in which two males have spastic paraparesis and Kallmann's syndrome (hypogonadotrophic hypogonadism and anosmia). One of the brothers also is color blind. The association of familial spastic paraplegia and Kallmann's syndrome has not been described previously.Keywords
This publication has 31 references indexed in Scilit:
- Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families.Journal of Neurology, Neurosurgery & Psychiatry, 1981
- X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg.Journal of Medical Genetics, 1976
- NEUROICHTHYOSIS WITH HYPOGONADSSM (RUD'S SYNDROME)International Journal of Dermatology, 1975
- Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism*Clinical Genetics, 1975
- Hypogonadotropic hypogonadism with anosmia--Kallmann's syndrome. A disorder of olfactory and hypothalamic functionArchives of internal medicine (1960), 1973
- Studies of the pituitary-Leydig cell axis in young men with hypogonadotropic hypogonadism and hyposmia: comparison with normal men, prepuberal boys, and hypopituitary patientsJournal of Clinical Investigation, 1969
- FAMILIAL CEREBELLAR ATAXIA AND HYPOGONADISMBrain, 1964
- ACUTE LEUKÆMIA AND KLINEFELTER'S SYNDROMEThe Lancet, 1961
- GENETIC FACTORS ON THE X CHROMOSOMEThe Lancet, 1961
- Hereditary cerebral palsy: A preliminary reportThe Journal of Pediatrics, 1957