ABSTRACT ID TITLE PRESENTER NAME
BHC-601 SEROPREVALENCE OF VIRAL TRANSFUSION TRANSMITTED INFECTIONS (HIV, HBV AND HCV) AND THEIR POSSIBLE CORRELATION WITH ABO AND RHD BLOOD GROUP TYPES IN BLOOD DONORS AT A TERTIARY CARE INSTITUTE IN HARYANA PAWAN SINGH
BHC-602 CLINICALLY SIGNIFICANT ANTI-M ANTIBODY IN AN M-POSITIVE INDIVIDUAL: A CASE REPORT WITH IMPLICATIONS FOR BLOOD TRANSFUSION MANAGEMENT SUSHREE DASH
BHC-603 AN UNSUAL PRESENTATION OF EXTRAMEDULLARY HEMATOPOIESIS IN A ADULT MANASWINEE MALLIK
BHC-604 BACTERIAL PATHOGENS CAUSING BLOODSTREAM INFECTION IN CANCER PATIENTS: ORGANISM PROFILE AND SUSCEPTIBILITY PATTERNS. HEMALI KADU
BHC-605 ACUTE FEBRILE ILLNESS IN MALNUTRITION - COCKTAIL FOR FATAL PATHOLOGY HITAKSHI GOEL
BHC-606 THE ENIGMA OF BIG SPLEEN DISEASE IN A CHILD-AN APPROACH TO CLINICAL DIAGNOSIS LAKSHINDER KAUR
BHC-607 WHY AM I GREY? ABHIJITH LAKSHMAN
BHC-608 UNUSUAL CASE OF SEVERE HEMOLYTIC ANEMIA DIVYA T
BHC-609 COMPARISON OF H-SCORE VS. 2004 CRITERIA FOR DIAGNOSIS OF HLH KOMAL KELA
BHC-610 HISTOPLASMOSIS IN AN IMMUNOCOMPETENT PATIENT: AN UNUSUAL PRESENTATION SUGANDHA SUMMAN
BHC-611 MOYAMOYA SYNDROME IN A SICKLE CELL DISEASE INDRANI MONDAL
BHC-612 A RARE SITE OF THROMBOSIS IN APLASTIC ANEMIA WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA MANASWINEE MALLIK
BHC-613 UTILITY OF MENTZER’S INDEX IN IDENTIFYING THALASSEMIA TRAIT IN RESOURCE POOR SETTINGS DIVYA DONEPUDI
BHC-614 A RARE BLEEDING DISORDER - : PROTHROMBIN DEFICIENCY BANUKEERTHANA RAJASEKARAN
BHC-615 BONE MARROW EXAMINATION IN THE DIAGNOSIS OF INFECTIOUS PATHOLOGY: AN OFTEN UNDERUTILIZED DIAGNOSTIC TOOL MONIKA MAHARJAN
BHC-616 AN UNUSUAL CASE OF CYTOMEGALOVIRUS (CMV) INDUCED NEUTROPENIA IN A 10 MONTH OLD MALE CHILD. SAURABH SINGH
BHC-617 SECONDARY HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN A BRUCELLOSIS PATIENT - A RARE CASE REPORT SONALIKA PRIYADARSHINI SAHOO
BHC-618 THE FROZEN CASTLE PRIYATHERSINI NAGARAJAN
BHC-619 HEMOSTATIC MANAGEMENT IN A CASE OF GLANZMANN’S THROMBASTHENIA WITH REFRACTORY GI BLEED CHAITANYA H BALAKRISHNAN
BHC-620 TRANSIENT ABNORMAL MYELOPOIESIS IN A DOWN’S SYNDROME BABY - A CASE REPORT SAPNA PATEL MC
BHC-621 GETTING EVEN WITH EVAN'S SUSHMA B
BHC-622 PARVOVIRAL INFECTION OF BONE MARROW MASQUERADING AS LYMPHOMA IN AN ANTI-PHOSPHOLIPID ANTIBODY (APLA) POSITIVE YOUNG MALE – A CASE REPORT SHEELA DEVI CS
BHC-623 BILATERAL ADRENAL HAEMORRHAGE IN A CASE OF ANTIPHOSPHOLIPID ANTIBODY SYNDROME – AN UNUSUAL PRESENTATION VERONICA LOBO
BHC-624 AGGRESSIVE HLH – A HAVOC IN DISSEMINATED TUBERCULOSIS SOUMYA KANTI MANDAL
BHC-625 A STUDY OF ANTIPROTHROMBIN / ANTIPHOSPHATIDYL SERINE ANTIBODIES IN PATIENTS OF PEDIATRIC SYSTEMIC LUPUS ERYTHEMATOSUS. SANJOLI CHUGH
BHC-626 HEMATOPATHOLOGICAL INSIGHTS INTO PITUITARY APOPLEXY SECONDARY TO PITUITARY ADENOMA GUTTIKONDA SATHVIK
BHC-627 BONE MARROW AMYLOIDOSIS (AMYLOID LIGHT CHAIN) PRESENTING AS MASSIVE SPLENOMEGALY IN THE ELDERLY. AN INTERESTING CASE REPORT. APARNA SINGH
BHC-628 PREVALENCE AND SPECTRUM OF HEMOGLOBINOPATHIES IN A TERTIARY CARE CENTRE OF UTTARAKHAND DIVYA KUMARI
BHC-629 ALL TMA IS NOT TTP, AMONGST OTHERS, CONSIDER MALIGANANCY! PANKHI DUTTA
BHC-630 AN UNUSUAL PRESENTATION OF DISSEMINATED TUBERCULOSIS ASSOCIATED WITH FLORID HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (HLH) SYNDROME KRITIKA DEWAN
BHC-631 DKMS BMST PATIENT FUNDING PROGRAM: GIVING HOPE FOR A HEALTHY FUTURE RESHMA KUMARI MV
BHC-632 MOLECULAR SPECTRUM OF INHERITED PLATELET DISORDERS RAJKUMAR VENKASTESAN
BHC-633 GENOMIC EVALUATION OF YOUNG PATIENTS WITH MYOCARDIAL INFARCTION BIPIN KULKARNI
BHC-634 SHADES OF HEMOLYSIS: AN UNUSUAL ENCOUNTER BETWEEN TRAITS AND ANTIBODIES SUMBUL MAZAHAR
BHC-635 A RARE OCCURRENCE OF HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN A SICKLE CELL DISEASE PATIENT LEADING TO UNFAVOURABLE NEUROSEQUELAE ARINDAM MANDAL
BHC-636 GSTA1 DIPLOTYPES INFLUENCE INTRAVENOUS BUSULFAN PHARMACOKINETICS IN CHILDREN WITH BETA-THALASSEMIA MAJOR UNDERGOING MATCHED ALLOGENEIC HAEMATOPOIETIC STEM CELL TRANSPLANTATION AGILA JAYARAMAN
BHC-637 A MODEL-INFORMED PRECISION OF ONCE-DAILY BUSULFAN DOSING IN PATIENTS UNDERGOING ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANTATION RAJESH NAGARAJAN
BHC-638 ROLE OF TRANSMEMBRANE SERINE PROTEASE 6 GENE VARIANTS ON PATHOPHYSIOLOGY OF IRON DEFICIENCY ANEMIA SANJAY PANDEY
BHC-639 CASE REPORT OF NIEMANN-PICK DISEASE TYPE A (NPD-A) MARY PUSHPA MURMU MURMU
BHC-640 DIAGNOSTIC OUTCOME OF BONE MARROW EXAMINATION IN VARIOUS HEMATOLOGICAL DISORDER: AN EXPERIENCE FROM TERTIARY CARE HOSPITALI VINITA PASWAN
BHC-641 EVALUATION OF RISK FACTORS COMPLICATING NONTRANSFUSION DEPENDENT THALASSEMIA. ANIL KUMAR DASH
BHC-642 PREVALENCE OF BETA THALASSEMIA TRAIT ATTENDING ANTENATAL CHECKUP IN A TERTIARY REFERRAL HOSPITAL ROMANCHIT UPADHYAYA
BHC-643 A COMPARATIVE COST ANALYSIS ASSESSING THE BURDEN OF COVID-19 ON PATIENTS UNDERGOING HEMATOPOIETIC STEM CELL TRANSPLANTATION AT A TERTIARY CARE CANCER CENTER IN EASTERN INDIA MANIK GHOSH
BHC-644 SICKLE CELL DISEASE WITH SYSTEMIC LUPUS ERYTHEMATOSUS -A RARE CASE REPORT FROM WESTERN ODISHA . BALKISHAN AGRAWALA
BHC-645 A CASE REPORT: VISCERAL LEISHMANIASIS (KALA-AZAR) HELEN TUDU
BHC-646 LAPAROSCOPIC SPLENECTOMY IN BETA THALASSEMIA MAJOR PATIENTS: PROS AND CONS - A SINGLE CENTRE STUDY SANIDHYA KUMAR MISHRA
BHC-647 THE AUTOIMMUNE HEPARIN?INDUCED THROMBOCYTOPENIA- FIRST CONFIRMED CASE IN INDIA PALLAVI PRAKHAR
BHC-648 RARE CASE OF COMPOUND HETEROZYGOUS FOR HEREDITARY PERSISTENCE OF FOETAL HEMOGLOBIN AND BETA THALASSEMIA MIMICKING THALASSEMIA INTERMEDIA. JAYITA DAS
BHC-649 ISOLATED MARROW TUBERCULOSIS - A HIDDEN CAUSE OF CYTOPENIAS. MADHUSMITA MANGARAJ
BHC-650 A USABILITY STUDY ASSESSING HANDLING AND PREFERENCE OF THE CONCIZUMAB PEN-INJECTOR IN PATIENTS WITH HAEMOPHILIA AND CAREGIVERS RANJAN KM
BHC-651 DYNAMICS OF STEM CELLS IN PERIPHERAL BLOOD (PB) DURING STEM CELL MOBILIZATIONS FOR STEM CELL TRANSPLANTATIONS, A SINGLE INSTITUTIONAL EXPERIENCE DEBI PRASAD JENA
BHC-653 LEISHMANIASIS IN A KNOWN CASE OF SICKLE CELL TRAIT WITH SECONDARY HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS – A RARE CASE REPORT MUKESH KUMAR PRADHAN
BHC-654 A CASE REPORT ON NUMB CHIN SYNDROME IN SICKLE CELL DISEASE PRATYUSH KUMAR PANDA
BHC-655 MANAGING INTRACRANIAL HAEMORRHAGE IN PATIENTS WITH HAEMOPHILIA: AN EXPERIENCE FROM A TERTIARY CARE CENTRE HARSHIT KHURANA
BHC-656 A RARE CASE OF ACUTE SOFT SKULL SYNDROME IN SICKLE CELL DISEASE PATIENT SUCHISMITA MISRA
BHC-657 CLINICAL PROFILE, TREATMENT PATTERNS AND QUALITY OF LIFE IN CANCER PATIENTS WITH VENOUS THROMBOEMBOLISM PRASHUN UPADHAYA
BHC-658 RARE PRESENTATION OF EXTENSIVE ERYTHEMATOUS MACULOPAPULAR SKIN LESIONS POST CLADRIBINE THERAPY IN HAIRY CELL LEUKEMIA (HCL). NEHA MOTWANI
BHC-659 CLINICAL PROFILE, TREATMENT PRACTICES AND RESPONSE IN PAROXYSMAL NOCTURNAL HEMOGLOBINURIA CASES GOUTHAM KRISHNA
BHC-660 RESPONSE OF RITUXIMAB IN STEROID RESISTANT IMMUNE THROMBOCYTOPENIC PURPURA - A RETROSPECTIVE STUDY LIPSA NAYAK
BHC-661 CEREBRAL VENOUS SINUS THROMBOSIS IN IMMUNE THROMBOCYTOPENIA PATIENTS TREATED WITH THROMBOPOIETIN RECEPTOR AGONIST: A CASE REPORT ADITYA DEBUKA
BHC-662 PRIMARY DIAGNOSIS OF LUPUS ERYTHEMATOSUS IN BONE MARROW GIFTA CATHARINE
BHC-663 ADULT-ONSET EVANS SYNDROME SHANTILATA SINGH
BHC-664 A RARE CASE OF SECONDARY IMMUNE MEDIATED THROMBOCYTOPENIA IN H.PYLORI POSITIVE PATIENT MANOJ KUMAR MALIK
BHC-665 A RARE ENCOUNTER: UNRAVELING A CASE OF THROMBOTIC THROMBOCYTOPENIC PURPURA SREENATH S
BHC-666 THREE CASES OF HYPEREOSINOPHILIC SYNDROME WITH CLONAL T CELLS AND DIFFERENT CLINICAL COURSES: A DIAGNOSTIC CONUNDRUM AISHWARYA KARTHIKEYAN
BHC-667 SPECTRUM OF HAEMOGLOBIN F (FETAL) AND HAEMOGLOBIN S (SICKLE) LEVEL IN SICKLE CELL HOMOZYGOUS PATIENTS (ARAB INDIAN HAPLOTYPE) ;IN SINGLE INSTITUTION EXPERIENCES RASHMI RANJAN BHOI
BHC-668 CHARACTERIZATION OF 40 NOVEL HLA CLASS I AND CLASS II ALLELES IDENTIFIED IN UMBILICAL CORD BLOOD (UCB) UNITS SUREKA RAJENDRAN
BHC-669 INFECTIONS IN BONE MARROW- AN INSTITUTIONAL STUDY MONALISHA NAYAK
BHC-670 PREVALENCE OF ACUTE TRANSFUSION ASSOCIATED COMPLICATIONS IN CHILDREN WITH ?-THALASSEMIA MAJOR IN A TERTIARY CARE CENTER IN NORTH INDIA: A PROSPECTIVE STUDY ALKA YADAV
BHC-671 STUDY OF INHIBITOR IN PWH- A RECEIVING F-VIII CONCENTRATION (PLASMA DERIVED) RENUKA SAHOO
BHC-672 AN UNUSUAL CASE OF GENERALISED LYMPHADENOPATHY WITH PURPURA IRSHAD ALI K M
BHC-673 UNUSUAL CASE PRESENTATION OF GAUCHER DISEASE IN AN ADULT METAANKSHA AHUJA
BHC-674 ISOLATED OSTEOSCLEROSIS VS LATE INACTIVE PAGET’S DISEASE- A DIAGNOSTIC DILEMMA. TANYA AGGARWAL
BHL-801 HBA2 LEVELS IN IRON DEFICIENCY - CAN IRON DEFICIENCY MASK THALASSEMIA SCREENING ? PREETI TRIPATHI
BHL-802 ASSESSMENT OF BLAST FLAG IN ADVIA 2120I CELL COUNTER BY PERIPHERAL BLOOD SMEAR EXAMINATION BABU PILLAI
BHL-803 MOLECULAR WORKUP IS ESSENTIAL IN BORDERLINE HAEMOGLOBIN A? ANJUMAN ASHOK
BHL-804 COMPARISON BETWEEN ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA) AND CHEMILUMINESCENCE IMMUNOASSAY (CLIA) FOR THE DETECTION OF TRANSFUSION TRANSMITTED DISEASE (TTD) MARKERS IN BLOOD DONORS MAYANK KUMAR
BHL-805 ASSESSMENT OF PERIPHERAL BLOOD SMEARS THAT WERE AUTOMATICALLY STAINED BY STAINZ PLUS TO THOSE THAT WERE MANUALLY STAINED IN A TERTIARY CARE FACILITY SWATI VAYKAR
BHL-806 APPLYING SIX SIGMA APPROACH TO MONITOR PERFORMANCE OF INTERNAL QUALITY CONTROL IN HEMATOLOGY LABORATORY OF A TERTIARY CARE CENTER – LESSONS LEARNT. SHIVALI SEHGAL
BHL-807 DIAGNOSTIC ACCURACY OF AUTOMATED FRAGMENTED RED CELL (FRC) COUNTING IN HEMOLYTIC ANEMIA-DO POIKILOCYTES AND MICROCYTES INTERFERE? RAJALAKSHMI RAJASHEKAR
BHL-808 APLASTIC ANAEMIA AS A RARE PRESENTATION IN HYPER-IGE SYNDROME (JOB SYNDROME) SWATI SHARMA
BHL-809 FLAER AS A STANDALONE DIAGNOSTIC REAGENT IN PAROXYSMAL NOCTURNAL HEMOGLOBINURIA TESTING: A CALL FOR GUIDELINE REASSESSMENT AND PRACTICE EVOLUTION PARVEEN BOSE
BHL-810 REFRIGERATION OF EDTA SAMPLES BETWEEN 0 TO 4 HOURS SHOWS THAT SAMPLES STAY VIABLE UPTO 24 HOURS FOR CBC ANALYSIS PRIYANK DOODANI
BHL-811 RENAL OSTEODYSTROPHY-BONE MARROW BIOPSY: A CASE REPORT ADITYA NARAYAN MONDAL
BHL-812 TO STUDY THE SPECTRUM OF RED CELL INDICES IN BETA THALASSEMIA ( TRAIT) PADMALOCHAN DWIBEDY
BHL-813 DIAGNOSTIC UTILITY OF PLATELET PARAMETERS FOR SCREENING OF DYSLIPIDEMIC PATIENTS SAYANTANI GHOSH HAZRA
MH-961 ASSESSING THE INFLUENCE OF FACTOR XIII VAL34LEU POLYMORPHISM IN INDIAN MYOCARDIALINFARCTION PATIENTS RAVI RANJAN
MH-962 UNLOCKING VEXAS SYNDROME IN INDIA: DECIPHERING CLINICAL AND LABORATORY PROFILES THROUGH A MULTIFACETED CASE SERIES AADYA KERKAR
MH-963 DUAL EFFECT OF HYDRALAZINE AS DEMETHYLATING AGENT OF CLOCK GENES AND DIFFERENTIAL REGULATOR OF ACUTE MYELOID LEUKAEMIA ASSOCIATED GENES. MINAKSHI SEN
MH-964 MODULATING EFFECT OF BCL11A (RS11886868) GENE VARIANT ON THE PHENOTYPE OF SICKLE CELL ANAEMIA PATIENTS: A TERTIARY CARE EXPERIENCE HARERAM PANDEY
MH-965 EXPLORING IGHV MUTATION STATUS AND STEREOTYPED SUBSETS IN CHRONIC LYMPHOCYTIC LEUKAEMIA (CLL): A COMPARATIVE STUDY USING SANGER SEQUENCING VERSUS CAPTURE BASED NEXT GENERATION SEQUENCING (NGS) SHRUTI CHAUDHARY
MH-966 A MULTIFACETED APPROACH TO ICF SYNDROME: INVESTIGATING KARYOTYPE, IMMUNOPHENOTYPING, AND MOLECULAR FINDINGS MANOJ V T
MH-967 SPECTRUM OF RARE GENETIC CAUSES OF INHERITED CYANOSIS: A CASE SERIES FROM A TERTIARY-CARE CENTRE AISHWARYA KARTHIKEYAN
MH-968 MUTATIONAL SPECTRUM OF NON-DELETIONAL ALPHA THALASSAEMIA IN TERTIARY CARE SETTING NEELAGANDAN KAMALANATHAN
MH-969 GENE DOSAGE QUANTITATIVE MULTIPLEX FLUORESCENT PCR AS A SCREENING TOOL FOR DETECTION OF DELETION IN DELTA-BETA THALASSEMIA SENTHIL KUMAR GOVINDA SWAMY
MH-970 PEDIATRIC AML WITH CONCOMITANT DDX41 & NPM1 MUTATION: AN EXTREMELY RARE ASSOCIATION PRATEEK DAS
MH-971 MYELOID NEOPLASMS WITH GERMLINE GATA2 MUTATION: A DIAGNOSTIC CONUNDRUM. PRATEEK DAS
MH-972 UNRAVELING IBRUTINIB RESISTANCE IN CHRONIC LYMPHOCYTIC LEUKEMIA: A CASE STUDY ON THE ROLE OF BRUTON TYROSINE KINASE MUTATION DEBAJANI NATHI
MH-973 A CASE OF CONGENITAL ERYTHROCYTOSIS CAUSED BY A NOVEL EGLN1 VARIANT – FIRST REPORT OF ECYT3 FROM INDIA KAJOL
MH-974 CYSTATIN F A POTENTIAL DIAGNOSTIC BIOMARKER IN ACUTE PROMYELOCYTIC LEUKEMIA HAMENTH KUMAR PALANI
MH-975 PREVALENCE OF JAK2V617F MUTATION, ITS ALLELE BURDEN IN HEPATIC VENOUS OUTFLOW TRACT OBSTRUCTION AND EXTRAHEPATIC PORTAL VENOUS OBSTRUCTION PATIENTS. A TERTIARY CARE CENTRE STUDY. SUMAN LATA
MH-976 NANO VARIANT OF BCR-ABL TRANSCRIPT PRESENTING WITH ATYPICAL FEATURES: A REPORT OF TWO CASES. PRATEEK DAS
MH-977 A RARE THREE-WAY COMPLEX TRANSLOCATION WITH VARIANT PHILADELPHIA CHROMOSOME T(4;9:22)(P16;Q34;Q11.2) IN A CHRONIC MYELOID LEUKEMIA PATIENT BIBHAS KAR
BHC-675 INTERESTING CASE OF SLE WITH REFRACTORY HYPOPLASTIC ANEMIA VINAYA GOPALASWAMY