[N-ras and fms gene mutation in idiopathic thrombocytopenic purpura and myelodysplasia].
Zhonghua Xue Ye Xue Za Zhi
; 29(3): 158-60, 2008 Mar.
Article
en Zh
| MEDLINE
| ID: mdl-18788612
ABSTRACT
OBJECTIVE:
To explore the pathogenesis of idiopathic thrombocytopenic purpura (ITP) and improve the differential diagnosis from myelodysplastic syndromes (MDS).METHODS:
Polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) was performed to detect the point mutation of codon 12,13 in N-ras gene and codon 301, 969 in fms gene in adult and aged ITP and MDS patients.RESULTS:
In 25 ITP patients, N-ras mutation and fms mutation were detected in one each (4%). Mutations were found in 3 of 8 MDS patients two (25%) with N-ras mutation and one (12.5%) with fms mutation.CONCLUSIONS:
Patients with N-ras or fms gene mutation diagnosed as MDS rather than ITP.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Síndromes Mielodisplásicos
/
Genes fms
/
Genes ras
/
Púrpura Trombocitopénica Idiopática
Límite:
Adult
/
Aged
/
Female
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Humans
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Male
/
Middle aged
Idioma:
Zh
Revista:
Zhonghua Xue Ye Xue Za Zhi
Año:
2008
Tipo del documento:
Article
País de afiliación:
China