A report of a probable case of familial Guillain Barre syndrome
Mohammad Barzegar, Amir Hossein Jafari Rouhi, Mehdi Farhoudi and 1 more
Annals of Indian Academy of Neurology · 2012
doi:10.4103/0972-2327.104341 (opens in a new tab)
We email you when a new notice or a question about this paper appears.
Abstract
Although it is a sporadic disease, few studies have reported cases of Guillain Barre Syndrome (GBS) in families which postulate a genetic susceptibility. Human leukocyte antigen (HLA) typing is an area of discussion in GBS though none of them are considered definitive. In recent years, more studies have evaluated HLA typing in sporadic cases while rarely it has been assessed in familial ones. We report a woman and her daughter experiencing GBS and their HLA typing in a 2-year interval.
Abstract licence: CC BY-NC-SA
References21
21 more references, whose wording the paper’s licence keeps private.
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.