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[A novel point mutation in the transmembrane domain of platelet glycoprotein IX gene identified in a Bernard-Soulier syndrome patient].

AbstractOBJECTIVE:
To diagnose a patient with Bernard-Soulier syndrome (BSS) and investigate her gene abnormality.
METHODS:
Platelet size and structure were studied under light and electron microscopies. Platelet membrane glycoproteins (GP) were measured by flow cytometry. PCR and DNA sequencing were used to identify gene abnormality.
RESULTS:
The patient had thrombocytopenia with giant platelets. Ristocetin-induced platelet agglutination was absent. GP I b/IX complex in the platelet membrane was significantly decreased, which was resulted from an Ala139 Thr substitution in the transmembrane domain of GPIX.
CONCLUSION:
Ala139 Thr mutation of the GPIX gene in this patient is a novel missense mutation, which has not been reported in BSS.
AuthorsZ Wang, J Shi, Y Han
JournalZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi (Zhonghua Xue Ye Xue Za Zhi) Vol. 22 Issue 9 Pg. 464-6 (Sep 2001) ISSN: 0253-2727 [Print] China
PMID11758225 (Publication Type: Case Reports, English Abstract, Journal Article)
Chemical References
  • Membrane Proteins
  • Platelet Glycoprotein GPIb-IX Complex
  • Ristocetin
  • Threonine
  • Alanine
Topics
  • Adult
  • Alanine (genetics)
  • Bernard-Soulier Syndrome (genetics)
  • Cell Size (genetics)
  • Female
  • Humans
  • Membrane Proteins (genetics, metabolism)
  • Platelet Aggregation (drug effects)
  • Platelet Glycoprotein GPIb-IX Complex (genetics, metabolism)
  • Point Mutation (genetics)
  • Protein Structure, Tertiary (physiology)
  • Ristocetin (pharmacology)
  • Threonine (genetics)
  • Thrombocytopenia (diagnosis, genetics)

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