Strumpell's disease in a family with hereditary focal segmental glomerulosclerosis.

Autor:	Efstratiadis G; Department of Nephrology, Hippokration General Hospital, Thessaloniki, Greece. efstrati@med.auth.gr, Memmos D, Tsiaousis G, Pantzaki A, Manou H, Logotheti V
Jazyk:	angličtina
Zdroj:	Renal failure [Ren Fail] 2006; Vol. 28 (4), pp. 351-4.
DOI:	10.1080/08860220600577767
Abstrakt:	Strumpell's familial spastic paraplegia is a rare hereditary disease, clinically characterized by progressive disturbance of gait. Focal Segmental Glomerulosclerosis (FSGS) is a frequent glomerulopathy, with an extremely rare familial subtype. The cases of two brothers with Strumpell' s disease are reported, who also developed glomerular renal disease, most probably familial FSGS. The genetics of the two disorders, Strumpell's paraplegia and familial FSGS, are discussed, together with the possibility of a parallel transmission.
Databáze:	MEDLINE
Externí odkaz:	Zobrazit plný text záznamu Plný text ve formátu PDF Plný text ve formátu HTML
Nepřihlášeným uživatelům se plný text nezobrazuje	K zobrazení výsledku je třeba se přihlásit.