Novel Heterozygous Mutations of Congenital Thrombotic Thrombocytopenic Purpura: A Rare Case Report.
Novel mutation
plasma infusion
secondary focal segmental glomerulo sclerosis
thrombotic thrombocytopenic purpura
Journal
Indian journal of nephrology
ISSN: 0971-4065
Titre abrégé: Indian J Nephrol
Pays: India
ID NLM: 8914356
Informations de publication
Date de publication:
Historique:
entrez:
20
8
2019
pubmed:
20
8
2019
medline:
20
8
2019
Statut:
ppublish
Résumé
Hereditary thrombotic thrombocytopenic purpura (TTP) is a genetic condition caused by mutations in
Identifiants
pubmed: 31423067
doi: 10.4103/ijn.IJN_241_18
pii: IJN-29-295
pmc: PMC6668320
doi:
Types de publication
Case Reports
Langues
eng
Pagination
295-297Déclaration de conflit d'intérêts
There are no conflicts of interest.
Références
Nature. 2001 Oct 4;413(6855):488-94
pubmed: 11586351
N Engl J Med. 2002 Aug 22;347(8):589-600
pubmed: 12192020
J Thromb Haemost. 2004 Mar;2(3):424-9
pubmed: 15009458
Hum Mutat. 2010 Jan;31(1):11-9
pubmed: 19847791
PLoS One. 2011;6(6):e21587
pubmed: 21720563
J Thromb Haemost. 2011 Jul;9 Suppl 1:283-301
pubmed: 21781265
Br J Haematol. 2014 Mar;164(6):759-66
pubmed: 24387053
Thromb Res. 2014 Dec;134(6):1171-5
pubmed: 25242241
BMC Hematol. 2014 Sep 12;14(1):16
pubmed: 25243071
J Thromb Haemost. 2018 Apr;16(4):618-629
pubmed: 29356300