Search Results - "Wan Ab Rahman, W S"

A rare case of compound heterozygous Southeast Asian double α-globin gene deletion and Haemoglobin Quong Sze in a Malay proband by Vijian, D, Wan Ab Rahman, W S, Kannan, T P, Zulkafli, Z, Mohd Noor, N H, Bahar, R, Hassan, M Z, Iberahim, S, Abdullah, M, Mohamed Yusoff, S, Ramli, M, Yasin, N, Esa, E

“…Haemoglobin (Hb) Quong Sze is a non-deletional α-thalassaemia subtype that occurs due to missense mutation at codon 125 of the HBA2 gene. Interaction between…”
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Sagittal sinus thrombosis in a patient with familial Protein C deficiency: Highlighting the impact of thrombophilia testing by Wan Ab Rahman, W S, Abdullah, W Z, Hassan, M N, Ahmed, S, Zulkafli, Z, Wan Ahmed, W A, Iberahim, S, Mohd Noor, N H

“…Plasma protein-C is a natural anticoagulant that inactivates factors Va and VIIIa. Familial protein C deficiency is inherited as an autosomal dominant…”
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Epidemiology, spectrum of clinical manifestations and diagnostic issue of acquired haemophilia: A case series by Wan Ab Rahman, W S, Abdullah, W Z, Husin, A, Nik Mohd Hassan, N F F, Hassan, M N, Zulkafli, Z

“…Acquired haemophilia A (AHA) is a rare acquired bleeding disorder caused by polyclonal immunoglobulin G autoantibodies against clotting factor VIII (FVIII)…”
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Familial antithrombin III deficiency in a Malay patient with massive thrombosis by Wan Ab Rahman, W S, Abdullah, W Z, Hassan, M N, Hussin, A, Zulkafli, Z, Haron, J

“…Patients with low antithrombin III (AT III) has increased risk for arteriovenous thromboembolic (TE) disease. We report a 28-year-old Malay lady who presented…”
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