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Bernard-Soulier Syndrome (BSS)is a rare hereditary disorder.Platelets in patients with BSS are unable to adhere, leading to an increased bleeding tendency. BSS cases are often misdiagnosed as idiopathic thrombocytopenic purpura (ITP). We report here a seven years old girl diagnosed as Bernard-Soulier syndrome with homozygous deletion of 39 nucleotides in the exon 2 of GP1BA. Bernard–Soulier syndrome should be considered before the patient is diagnosed with immune thrombocytopenia.
[Lina Ahmed Wasfi, Abdul Rahman Hassan Issa, Shatha Ahmad Awad Aljuhani, Ruaa Omar Nughays, Walaa Mohammed Hafez Hassan and Tyseer Hassan Ahmed Hassan (2018); A CASE REPORT OF BERNARD-SOULIER SYNDROME IN DIFFERENTIAL DIAGNOSIS OF IMMUNE THROMBOCYTOPENIC PURPURA Int. J. of Adv. Res. 6 (1). 120-130] (ISSN 2320-5407). www.journalijar.com
Article DOI: 10.21474/IJAR01/6193 DOI URL: http://dx.doi.org/10.21474/IJAR01/6193
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