8th Thalassemia Lunch-On Symposium - MHG INDIA
In association withYouth Thalassemia AllianceMumbaiThalassemia & Sickle Cell Societyof Bangalore, BengaluruThalassemic GujaratAhmedabad8th ThalassemiaLunch-OnSymposiumSaturday, 12th October 2019Venue:S P Jain AuditoriumBombay Hospital,Marine Lines, MumbaiThalassemia Society Pune ChapterPuneLet's Help Some1VaranasiVivekanand Youth ClubRajkotTHALASSAEMIAAll roads lead to cureThalassemia Society of GoaGoaUnder the aegis ofMumbai Hematology GroupThalassemia & Sickle Cell SocietyHyderabadSupported byLink for ter/8thThalasym
With compliments fromMumbai Hematology GroupExecutive CommitteePresidentM.B. AgarwalVice-PresidentFarah JijinaSecretaryRucha PatilTreasurerSubhaprakash SanyalMembersShubhangi AgaleS.D. BanavaliRoshan ColahS. KhodaijiVrinda KulkarniMamta ManglaniNavin KhattryChandrakala SAsha ShahShrimati ShettyTHALASSAEMIAAll roads lead to cure
Know our facultyInternationalDr Maria-Domenica Cappellini She is Full Professor of Internal medicine, University of Milan, Italy (Department of ClinicalSciences and Community Health) for last 20 years Since 2016, she is Chief of ‘Rare Diseases Centre’ in Milano, Italy Since 1999, she has been the chief of ‘thalassemia and hemoglobinopathies centre’,Milano, Italy She has done extensive research in the field of hereditary disorders of red cellsspecially thalassemia She is an invited speaker and chair for various prestigious meetings and events across the globe She was president of European Federation of Internal Medicine She is member of American Society of Hematology, European Society of Hematology,Italian Society of Hematology & Italian Society of Internal Medicine She is scientific Advisor for the Thalassaemia International Federation (TIF) andcontributor to their meetings She was instrumental in establishing the guidelines for the treatment of thalassemiapublished by TIF She was sectional editor for Thalassemia Intermedia Section inEuropean Journal of Internal Medicine (EJIM) She is a member of editorial board of the prestigious hematology journal - Hematologica She did fellowship in MRC Molecular Hematology Unit -John Radcliffe Hospital Oxford,England (1981-83) She was also a visiting scientist in the same unit during 1983 - 87 forvarious cooperative projects She has published extensively (over 100 peer reviewed papers invarious international journals of great reputeTHALASSAEMIAAll roads lead to cure
Scientific Agenda08.30 amRegistration and coffee09.00 amWelcome address: Dr M B Agarwal09.10 amIntroduction of guest speaker: Dr Rucha PatilSession 1Chair: Dr Rashmi Dalvi, Dr Ajit Gorakshakar, Dr Sameer Tulpule09.15 amCase - 1Title: Thrombosis in Hb E Beta ThalassemiaSpeaker: Dr Anand Bodade, Ex-Registrar in HematologyMentor: Dr Vrinda KulkarniFrom: T N Medical College and BYL Ch Nair Hospital, Mumbai09.30 amGuest lecture - 1Title: Thalassemia intermedia: A few clinical issuesSpeaker: Dr Subhaprakash Sanyal, Hematologist,Hemato- Oncologist & Bone marrow transplant physicianFrom: Dept of Hematology, Fortis Group of Hospitals, MumbaiSession 2Chair: Dr Shrimati Shetty, Dr Mukesh Sanklecha, Dr Vrinda Kulkarni09.45 amCase - 2Title: NTDT with increased transfusion requirement - 2 casesCase presenter: Ritika Khurana, PHO FellowFrom: B J Wadia Hospital for Children, Parel, Mumbai10.00 amCase - 3Title: Case of Hyperhemolysis in bthalassemia intermediaCase presenter: Col (Dr) Rajiv Kumar, Clinical HematologistFrom: INHS Asvini, MumbaiSession 3Chair: Dr Chandrakala S, Dr Priti Mehta, Dr Suman Jain10.15 amCase - 4Title: Allo-immunization in thalassemia intermedia - How to manage ?Case presenter: Dr Muralidaran C, 2nd year, DM Resident,From: Dept of Hematology, KEM Hospital, Parel, Mumbai10.30 amCase - 5Title: Transfusion dependent bThalassemia trait - A mystery unveiledCase presenter: Dr Liza Bulsara, FellowFrom: MCGM - Comprehensive Thalassemia Care,Pediatric Hematology-Oncology & BMT Centre, Borivali, Mumbai10.45 amOpening ceremony11.00 amCoffeeSession 4Chair: Dr Sujata Sharma, Dr Ratna Sharma, Dr Archana Jiwane11.25 amGuest lecture - 2Title: Current scenario of care & control of thalassemia in India: The roadmap aheadSpeaker: Dr Roshan Colah, Former Director In-Charge, NIIH, Mumbai11.35 amGuest lecture - 3Title: Exploring pain in thalassemiaSpeaker: Dr Shruti Kakkar (Ahuja), Assistant ProfFrom: Dept of pediatrics, Dayanand Medical College & Hospital, LudhianaTHALASSAEMIAAll roads lead to cure
Scientific Agenda.cont'dSession 5Chair: Dr Sangita Lodha, Dr Santanu Sen, Dr Purvi Kadakia11.55 pmCase - 6bTitle: Association of dthalassemia with bthalassemia:Clinical, Hematological and Molecular aspects.Case presenter: Dr Priya Hariharan, PhD student, NIIH, Mumbai12.10 pmCase - 7Title: HbA2 Saurashtra: A dGlobin Chain Variant that can mask the diagnosis ofbthalassemia traitCase presenter: Ms Manisha N Daruwalla, Section Technical ManagerCo-authors: Dr Kainaz Sidhwa, Dr Ravikiran Pawar, Dr Priya Hariharan,Dr Anita Nadkarni1 & Dr Amar DasguptaFrom: Sections of Hematology, Coagulation and Flow CytometrySRL Diagnostics and 1National Institute of Immunohematology, Mumbai, IndiaSession 6Chair: Dr Archana Swami, Dr Ruchira Misra, Dr Omkar Khandkar12.25 pmCase - 8Title: Role of hydroxycarbamide in dbThalassaemiaCase presenter: Dr Sneha Waghela, Fellow - Pediatric Hematology-OncologyFrom: LTM Medical college, Sion, Mumbai12.40 pmGuest lecture - 4Title: Our experience of transplanting over 30 pediatrics thalassemicsSpeaker: Dr Santanu Sen, Consultant in Paediatric Oncology & BMTFrom: Kokilaben Dhirubhai Ambani Hospital, Andheri, Mumbai12.55 pmLunchSession 7Chair: Dr Shubhangi Agale, Dr K Pitchi Reddy, Dr Rajesh Patil01.35 pmGuest lecture - 5Title: Cardiac Iron Overload - Is IV Chelation an Option?Speaker: Dr Mamta Manglani, DirectorFrom: MCGM - Comprehensive Thalassemia Care,Pediatric Hematology-Oncology & BMT Centre, Borivali, MumbaiSession 8Chair: Ms Sangeeta Wadhwa, Mr Pankaj Sethi, Ms Chandni Jadhwani01.50 pmPresentation from patients, parents & well wishers1. Ms Pooja Gupta: The secrets of my success2. Ms Jharana Mallick: Listen, learn and then . lead !3. Mr Sunil Dubey: You dare to disagree4. Mr Rohit Roy: The difference between winning and succeeding5. Mr Ajit Vahadane: I will like to start a movement6. Mr Imran Mohammed Ali : Turning pain in to blessing7. Ms Aditi Rokade: Blood donationSession 9Chair: Dr M B Agarwal, Mr Gagan (Sunny) Chandok03.30 pmGuest lecture - 6Title: Tips for improved care of thalassemicsSpeaker: Dr Maria-Domenica Cappellini, Italy04.45 pmVote of thanks: Dr Rucha Patil05.00 pmHigh teaTHALASSAEMIAAll roads lead to cureDr Rucha Patil, PhDDr M B AgarwalScientist B, NIIHSecretaryMumbai Hematology GroupPresidentMumbai Hematology Group
In association withYouth Thalassemia AllianceMumbaiThalassemia & Sickle Cell Societyof Bangalore, BengaluruThalassemic GujaratAhmedabadThalassemia Society Pune ChapterPuneLet's Help Some1VaranasiVivekanand Youth ClubRajkotThalassemia Society of GoaGoaThalassemia & Sickle Cell SocietyHyderabadMumbai Hematology GroupHematology Centre, Ghamat Lodge, 804-A,Dr. B. Ambedkar Road, Dadar TT, Mumbai 400014.Email ID: mbagarwal1@gmail.comWebsite : www.mhgindia.comLink for registration: ym
Chair: Dr Shrimati Shetty, Dr Mukesh Sanklecha, Dr Vrinda Kulkarni Title: NTDT with increased transfusion requirement - 2 cases . Chair: Dr Archana Swami, Dr Ruchira Misra, Dr Omkar Khandkar Title: Role o
thalassemia mostly occurs from point mutation. There are two types of beta thalassemia i.e β and 0-thalassemia which reduce amount or absence of β-globin production, respectively. Homozygous β0-thalassemia ( 0/ 0) and some / 0 cases cause severe thalassemia while homozygous β -thalassemia ( β / ) moderate severity.
Sickle beta thalassemia (also called sickle cell thalassemia disease) his is also a form of sickle cell disease. ells may have a tendency to change from a round shape to a sickle shape. n people with sickle beta thalassemia, one parent has sickle cell trait and the other parent has thalassemia trait. II. Background
beta‐thalassemia major would have short life expectancies of about one to eight years old. Beta‐thalassemia major is the more serious condition of the two and is also more likely to have greater implications in the workplace. For this is the reason, the report focuses
SCD/Thalassemia and COVID-19: Possible Risks and a Proposal for a Patient . At the beginning of the pandemic all our Thalassemia and sickle cell disease patients had been advised by phone calls, email, or directly at the center to . 58% report severe shortages ; .
cient beta-globulin thalassemia. This condition also is referred to as Cooley’s anemia or Mediterranean anemia. Both Africans and African-Americans also have an increased incidence of thalassemia. The incidence of thalassemia varies worldwide; however, more than 1,500 people in the United States are affected and 2 million carry the
Essays on Modern Japanese Thought. 4,2 Symposium: Japan in the 1970's. 5,2 Symposium: Translation and Japanese Studies. Introduction by Roy Andrew Miller. 6,1 Symposium on Japanese Society. Introduction by Susan B. Hanley. 8,1 Symposium on Ie Society. Introduction by Kozo Yamamura. 11,1 Symposium: Transition From Medieval to Early Modern Japan.
a. biography b. mystery c. fantasy d. fable 6. Which sentence is true, according to the story? a. Emma pulled prunes out of her lunch bag. b. Alice’s mother visited her daughter at lunch. c. Emma’s lunch bag had more food in it than usual. d. Alice smiled when she pulled an apple out of her lunch bag. Emma’s Lunch Surprise By Anita N. Amin
www.schoolpaymentsolutions.com. If preferred, students may bring a cold lunch; however, Students are not allowed to bring soda pop to drink with their lunch. In case of forgotten lunch or lunch money, we will allow the student to charge a lunch, although this is against district policy. We will not allow a child to go without lunch.
