x

Like our Facebook Page

   
Early Times Newspaper Jammu, Leading Newspaper Jammu
 
Breaking News :   Suspension of Indus Water Treaty could lead to hunger, thirst in Pakistan, admits Minister | VPN usage banned in Doda after suspected movement of terrorists | Jammu Cong leaders concerned over controversial remarks by Kashmir colleagues | Centre bans import of goods from Pak; prohibits vessels; blocks postal services | CM Omar calls on PM Modi | Border skirmishes continue for 9th day | Take stand against perpetrators: Farooq urges J&K people | NIA obtains Rana’s voice, handwriting samples | CRPF dismisses jawan for concealing his marriage with Pak Woman | ACB arrests Incharge PP GMC Jammu, his driver | Empowering Youth: 67 cases of Mission Youth schemes approved | ACB arrests Incharge PP GMC Jammu, his driver | Dal Lake Boat Capsize Youth’s body recovered | Rajnath set to skip Russia’s ‘Victory Day Parade’ | NMC cancels admission of 14 students, orders suspension of 26 more | Power Shut down | DC Reasi inspects ongoing cleanliness of water structures | U-14 boys compete in Carrom, Chess, Badminton, Yoga & Wrestling | Bandipora Legislators discuss roadmap for district | Desh Bhagat Global School NCC Navy Cadets Excel at Annual Training Camp | Training program on PMAY-U 2.0 held | Seminar on ‘Drug Addiction: A Curse’ held | GBHSS Rajouri organises maiden INTROFEST 2025 | Sadhotra exhorts women to play role in societal transformation, combating drug menace | Operation of 3 medical stores suspended for violating conditions of licences | WAVES 2025: Radio's Digital Future with Analog Coexistence Stressed by Global Experts | Union Minister of State Dr L Murugan honours 12 Community Radio Stations for their outstanding contributions | Nations adopt WAVES declaration to champion heritage, creativity, and collaboration in AI era | Netflix CEO Ted Sarandos Discusses Impact of Streaming on Indian Filmmaking at WAVES Summit | Centre's ban on Pakistan trade a strategic move post-Pahalgam Attack: Kavinder | Panun Kashmir urges Government to declare Pakistan a terrorist state | JMC allots modern kiosks and rehris to registered vendors | Rotary Club donates school supplies, inspires youth to give back | DC, SSP chair civil society meeting to address local developmental issues | MIER College of Education hosts Theatrical Tribute to Samuel Beckett's Legacy | Donation box theft case at temple solved by Jammu Police | Samba police seizes five vehicles for illegal mining activities | BBIA Club inaugurated by Samba Deputy Commissioner | GCW Udhampur NCC Cadets Excel at CATC Camp | GDC RS Pura hosts Poster Display on Viksit Vibrant Village Program | Kuldeep Gupta to represent AKF at Asian Youth Games 2025 technical meeting | Jaypee University hosts HR Conclave 2025 to strengthen academia-industry synergy | LPU's class of 2025 bids farewell with cheers, tears, and beats | GDC Ramgarh observes World Press Freedom Day | GDC Ganderbal organises annual road race | Back Issues  
 
news details
World Thalassemia Day 2018: 8 facts about this genetic disorder that will shock you
5/8/2018 12:26:19 PM
Agencies
India is suffering from the burden of Thalassemia, a genetic disorder, characterised by abnormal formation of haemoglobin which further causes improper transport of oxygen and destruction of red blood cells. Thalassemia causes people to have fewer red blood cells and suffer from anaemia.
This genetic disorder carries some worrisome statistics for patients of India as very recently according to an alarming report by the World Health Organisation (WHO), about 90% of thalassemic people from the western countries lead quite a normal life whereas almost half of the thalassemic patients in India die before they reach adulthood.

Here are more facts about the genetic disorder, Thalassemia on World Thalassemia Day that you should know:

About 3.9 % of India’s population is a carrier for thalassemia. More than 10,000 thalassemic children born every year in India.
Talking about Thalassemia and its effects on pregnancy experts say that there are about 9 million pregnant carriers every year and almost about 56000 infants have major thalassemia out of which 30000 need a regular transfusion.
People having family members in certain parts of the world like Asia, middle east, Africa, moreover Mediterranean countries like Turkey and Greece have a greater risk of developing Thalassemia.
Thalassemia is almost unpreventable as is hereditary and is passed from parents to children. However, there are vaccinations available and you might want to keep a check on your child’s vaccination schedule.
While treatment depends on the type of thalassemia a patient is suffering from, the most common treatment for thalassemia is a regular blood transfusion.
People suffering from Alpha thalassemia are silent carriers and generally, have symptoms of the disorder.
Regular blood transfusions can result in iron to build up in the blood also called the iron overload and can damage organs like heart and liver. Iron overload-induced heart diseases are the main cause of death among thalassemia patients.
Bone problems like osteoporosis are very common in thalassemia patients.
  Share This News with Your Friends on Social Network  
  Comment on this Story  
 
 
 
Early Times Android App
STOCK UPDATE
  
BSE Sensex
NSE Nifty
 
CRICKET UPDATE
 
 
 
 
 
 
 
 
   
Home About Us Top Stories Local News National News Sports News Opinion Editorial ET Cetra Advertise with Us ET E-paper
 
 
J&K RELATED WEBSITES
J&K Govt. Official website
Jammu Kashmir Tourism
JKTDC
Mata Vaishnodevi Shrine Board
Shri Amarnath Ji Shrine Board
Shri Shiv Khori Shrine Board
UTILITY
Train Enquiry
IRCTC
Matavaishnodevi
BSNL
Jammu Kashmir Bank
State Bank of India
PUBLIC INTEREST
Passport Department
Income Tax Department
JK CAMPA
JK GAD
IT Education
Web Site Design Services
EDUCATION
Jammu University
Jammu University Results
JKBOSE
Kashmir University
IGNOU Jammu Center
SMVDU