Vol. 2 No. 2 (2017): Special Issue (Dec 2017)

Extended Abstracts for GG2020 Conference 2017

• Molecular Identification of a Rare Haemoglobin Variant: Hb G Coushatta in Malaysia

  Alifah Nadia Abu Hassan, Ezalia Esa, Nur Aisyah Aziz, Faidatul Syazlin Abd Hamid, Siti Aisyah Lazim, Zubaidah Zakaria

  1-2

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• Complex Chromosomal Rearrangement der(5)ins(5;3)(q31;q25q29), t(3;12)(q24;p12.2) In A Dysmorphic Child, - A Case Report

  Aziati Azwari Annuar, Nik Mohd Zulfikri Mat Zin, Siti Mariam Ismail, Nurul Alia Mohd Nawi, Nazihah Mohd Yunus, Iluni Hayati Ibrahim, Sarina Sulong, Zilfalil Alwi, Ravindran Ankathil

  3-5

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• Globin Gene Defects in Normal and Borderline Haemoglobin A2 Levels: An IMR Experience

  Durar Aqilah Zamri, Lailatul Hadziyah Mohd Pauzy, Ezalia Esa, Yuslina Mat Yusoff, Nur Aisyah Aziz, Syahzuwan Hassan, Faidatul Syazlin Abdul Hamid, Zubaidah Zakaria

  6-7

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• Exploring the Willingness for Carrier Screening among Extended Family Members of a Thalassaemia Carrier Individual: A Lesson Learned

  Edhyana Sahiratmadja, Ani Melani Maskoen, Dadang Sjarief Hidajat Effendy, Ramdan Panigoro

  8-10

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• Four nucleotide deletions of exon 47 in Dystrophin gene: A case report of a Kelantanese Duchenne Muscular Dystrophy patient

  Fatimah Azman, Rose Adzrianee Adnan, Norhafizah Che Abdul Razak, Rozita Abdullah, Nazihah Mohd Yunus, Teguh Haryo Sasongko, Sarina Sulong, Zilfalil Alwi

  11-13

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• Isolation of Peripheral Blood Nucleated Red Blood Cells from β-Thalassaemia Patients Using CD71 Magnetic Activated Cell Sorting

  Haiyuni Mohd Yassim, Heba Ali, Rosline Hassan, Wan Zaidah Abdullah, Muhammad Farid Johan

  14-16

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• DNA Methylation of IGSF4 gene as an Epigenetic Modifier in HbE/β-Thalassaemia

  Haiyuni Mohd Yassim, Wan Zaidah Abdullah, Muhammad Farid Johan

  17-19

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• Azacytidine Enhances Sensitivity Response to Imatinib in BCR/ABL positive CML Cell Line

  Hamid Ali Nagi Al-Jamal, Wan Rohani Wan Taib, Siti Asmaa Mat Jusoh, Aziee Sudin, Muhammad Farid Johan

  20-22

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• Case Series of Homozygous and Compound Heterozygosity of Hb Malay, the Diagnostic Features and Transfusion Requirements

  Hanizah Salwa Amran, Nurimatussolehah Sarijan, Jameela Sathar Sathar, Sabariah Md Noor

  23-25

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• Haemolytic Disease of Foetus and Newborn and Haemolytic Transfusion Reaction Due to Kidd Antibody in Hospital Umum Sarawak, Malaysia

  Irni Mohd Yasin, Narazah Mohd Yusoff, Afifah Hassan, Muhammad Masrin Md. Zahrin

  26-27

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• Genetic Variants in HBS1L-MYB rs9399137 and rs11759553 Associated with Elevated HbF Levels Among Filipino β°-deletion Carriers

  Lai Kuan Teh, Koh Sam Yu, Shi Min Chua, Elizabeth George, Mei I Lai, Lily Wong

  28-29

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• Assessing Knowledge About Thalassemia Among Reproductive Age Population After Video Media Education

  Lulu Eva Rakhmilla, Ranisa Larasati, Edhyana K. Sahiratmadja, Enny Rohmawaty, Susi Susanah, Sjarif Hidayat Effendi

  30-32

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• A Pilot Study on the Willingness of Premarital Malays on Premarital Thalassaemia Screening

  Nor Ezzati Nor Albashri, Noor Fadzilah Zulkifli, Asral Wirda Ahmad Asnawi, Zetty Nadia Mohd Zain, Rashidah Mohamed, Jameela Sathar, Ainoon Othman

  33-34

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• Evaluation of Heterozygous Hb E and Its Interaction with Deletional Alpha Thalassaemia in Kelantan

  Nur Hidayah Muhamad Yasin, Majdan Ramli, Ilunihayati Ibrahim, Rosnah Bahar, Noraesah Mahmud, Siti Shahrum Muhamed Said, Wan Norhasanah Wan Yusoff, Marini Ramli

  35-37

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• Association of -582 A> G HAMP-P Polymorphism and Iron Status of Javanese β Thalassaemia Carriers

  Nyoman Suci Widyastiti, Harianto Notopuro, Catharina Suharti, Aryati Aryati

  38-39

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• Von Willebrand Factor Profiles of the Different ABO Blood Groups Among Malay Population

  Rohaida Abd Rahman, Faridah Afandi, Tun Maizura Mohd Fathullah, Rafeezul Mohamed

  40-41

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• Detection of XMN1-Gγ Polymorphism Among Patients with HbE/Î’eta Thalassaemia in North East Malaysia

  Rose Adzrianee Adnan, Nor Sarifah Hanafi, Zilfalil Alwi, Sarina Sulong

  42-43

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• Co-inheritance of Southeast Asian Ovalocytosis and Hb E: Does it affect the red blood cells indices?

  Shahrzard Riahi, Mei I Lai, Elizabeth George, Ida Marhainis Isahak, Faridah Idris, Sabariah Md Noor

  44-46

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• Hematological Parameter Evaluation in Different Types of Deletional Alpha-Thalassemia in Hospital Universiti Sains Malaysia

  Samilawati Mohd Arifin, Marini Ramli, Rosnah Bahar

  47-48

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• Hb E Syndrome with co-inheritance of Hb H-Constant Spring and Compound Beta Thalassaemia: A Diagnostic Challenge

  Wan Zuhairah Wan Embong, Rosnah Bahar, Wan Zaidah Abdullah, Marini Ramli, Noor Haslina Mohd Noor, Shafini Mohamed Yusoff

  49-51

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• The Haemoglobin G Makassar (Codon 6 GAG>GCG) Cases in Malaysia: Molecular Identification and Characterization

  Sok Fang Khor, Ezalia Esa, Nur Aisyah Aziz, Faidatul Syazlin Abdul Hamid, Yuslina Mat Yusoff, Zubaidah Zakaria

  52-53

  • 52-53

• An Alternative Method for Rapid Detection of Alpha Thalassaemia Variants in Malaysia using Droplet Digital PCR

  Tze Yan Lee, Elizabeth George, Mei I Lai, Vasudevan Ramachandran, Jin Ai Mary Anne Tan, Lai Kuan Teh, Raudha Othman, Nor Hidayat Hussein

  54-56

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• Attention and Executive Function Impairment in Children with Beta-Thalassaemia Major

  Uni Gamayani, Popon Gartika, Luh Putu Meidha, Aih Cahyani, Siti Aminah Siti Aminah, Ramdan Panigoro

  57-59

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• Effect of transfusion, iron chelation and splenectomy therapies in HbE/β-thalassaemia individuals in Malaysia

  Wai Feng Lim, Logeswaran Muniandi, Elizabeth George, Jameela Sathar, Lai Kuan Teh, Mei I Lai

  60-61

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• A Cross Sectional Assessment of Health-related Quality of Life among Patients with Thalassaemia in Malaysia

  Wan Ismahanisa Ismail, Mohamed Azmi Ahmad Hassali, Maryam Farooqui, Fahad Saleem, Wan Rohani Wan Taib, Muhammad Nabil Fikri Roslan

  62-63

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• Coinheritance of Beta Thalassaemia (β0 Filipino) and Delta Variant (HbA2 Deventer) in Sabahan Population: A Case Series

  Yuslina Mat Yusoff, Syahzuwan Hassan, Nizmah Mahani Mokhri, Nur Aisyah Aziz, Faidatul Syazlin Abdul Hamid, Ezalia Esa, Rahimah Ahmad, Zubaidah Zakaria

  64-65

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