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Corruption and combat aircraft
India’s security can’t be compromised
by G. Parthasarathy
At a time when the credibility of the Manmohan Singh government lies in tatters thanks to the scandal related revelations it faces on corruption, the recent announcement by the government, narrowing the list of qualified bidders, on the acquisition of 126 Medium Multi-Role Combat Aircraft (MMRCA) has happily not invited any accusations for corruption, cronyism or nepotism. This is unquestionably because of the impeccable reputation for honesty and probity that Defence Minister A.K. Anthony enjoys in India and abroad. But many like former National Security Adviser Brajesh Mishra aver that our defence procurement procedures are “antiquated and excessively time-consuming”.They argue that Mr Anthony’s fixation with his image of impeccable honesty (he is often jocularly referred to as Saint Anthony!) has resulted in serious delays in the procurement of vital defence equipment, ranging from Army helicopters and 155 mm Howitzers to combat aircraft and submarines. Mr Mishra warns that our defence planners have to note that since 2008 the Sino-Pakistan “all-weather friendship” has become a “military alliance directed against India,” for which “we may have to defend ourselves at the same time”. The IAF has a sanctioned strength of 39.5 combat squadrons. Barely 29 squadrons are operational at present. Some of these are equipped with the aircraft of the 1960s and 1970s vintage. Even with scheduled acquisitions, we will reach a level of 39.5 squadrons in 2017. We will then find that given the Sino-Pakistan alliance, the IAF requires a minimum of 45 combat squadrons. Pakistan’s Air Force (PAF) presently has 22 combat squadrons. It is set to acquire 10 to 12 squadrons of JF 17 and a couple of squadrons of J10 fighters from China. The latter is an Israeli variant of the American F16. The Chinese Air Force (PLAAF) already has 350 “fourth generation” fighter aircraft and is set to have an estimated 300 frontline combat aircraft based in the Lanzhou and Chengdu Military Regions bordering India. Despite these developments, we have proceeded at a rather leisurely pace with our defence modernisation, though in its growing fleet of Russian Sukhoi 30s, the IAF has one of the finest contemporary fighters. India has adopted a transparent process of tendering for acquiring the MMRCA. The bids came from Russia (MiG 35), Sweden (Grippen), France (Rafale), the US (F16 IN and FA 18 E/F Super Hornet) and the European Eurofighter Consortium comprising Germany, the UK, Italy and Spain for the Eurofighter “Typhoon”. Over the past two years, dozens of senior IAF officials have gone through each of these bids meticulously to see how far they fulfilled the 643 parameters the IAF had laid down. The aircraft offered have been put through rigorous flight tests in Leh (high mountainous terrain), Jaisalmer (hot desert terrain) and Bangalore, across the coastal belt. A high-level Technical Evaluation Committee laid down guidelines for offsets India expects from manufacturers, with they also required to effect substantial and substantive transfer of the aircraft’s technology, in an effort to boost India’s aerospace industry, which lags seriously behind its Chinese counterpart. Following the earlier rejection of the Grippen and MiG-35 bids, New Delhi recently announced that both American aircraft, the F/16 IN and F/A18 E/F, also failed to meet IAF requirements. The Americans argued that their fighters alone possess the unquestionably superior AESA radar, which gives them a combat edge. More importantly, the Americans have looked at the entire MMRCA acquisition in larger strategic terms. American analyst Ashley Tellis, whose knowledge of Indian defence and nuclear policies is profound, asserted: “The winner (of the MMRCA contract) will obtain a long and lucrative association, with a rising power and secure a toehold into other parts of India’s rapidly modernising strategic industries. The aircraft will play a vital role in India’s military modernisation as the country transforms from a regional power to a global giant”. There is “disappointment” in Washington at the rejection of American bids, more so as President Obama had personally lobbied with Prime Minister Manmohan Singh on this issue. Hopefully, the Americans will understand that on issues like the acquisition of the MMRCA, India will not yield to external pressures. Even the Americans acknowledge that both aircraft they offered are of relatively old vintage and cannot be upgraded any further. On the other hand, both the Eurofighter and the French Rafale are relatively new and can be upgraded substantially in future. With Pakistan already flying F16s for over a quarter of a century, there was little enthusiasm for the F16 IN offered, even though it is a much more advanced version of what the PAF flies. The F/A18 E/F failed in high altitude flight trials in Leh in early 2010. Its acquisition would have put the IAF at a disadvantage when facing the PLAAF. In some flight evaluations, the Grippen performed better than the F/A 18. Moreover, India has found US conditions of “end use monitoring” of the equipment the US supplies irksome, if not demeaning. Serious doubts also remain about American readiness for transfers of technology, which could substantially benefit our aerospace industry. The US has little reason to complain when it loses out in the face of international competition. Defence contracts with India, especially during Mr Anthony’s tenure, have been substantial and included 6 C 130 J Super Hercules, 10 C 17 Globemaster Transport aircraft and 12 Poseidon Maritime Reconnaissance Aircraft, apart from the troop-carrying ship “Trenton”. India is also set to purchase a substantial number of light Howitzers for its Mountain Divisions and consider an offer of 197 helicopters for the Army from the US after having scrapped a deal with Eurocopter following American protests. Equally, there is no cause for our worthy communists, who never tire of espousing the cause of the Chinese, while turning a blind eye to Sino-Pakistan nuclear and military cooperation, to celebrate Mr Anthony’s decision. Mr Anthony has handed out more high value defence contracts to the Americans than any of his predecessors. The Ministry of Defence appears to have understandably decided that cost will not be the primary consideration in the selection of the MMRCA. The Eurofighter was sold to Saudi Arabia at a cost of $ 123 million per aircraft - more than double that of its Americana and Russian competitors. The Rafale, priced at around $ 85 million, is also substantially costlier than its American and Russian competitors. The Eurofighter deal with Saudi Arabia was clouded with serious allegations of corruption and kickbacks. This should not be repeated in its dealings in
India.
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OPED
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In India approximately 30,000 Down syndrome babies are born annually. Prenatal screening for chromosomal abnormalities is highly essential for socio-economic growth and development of the country
Test early for genetic disorders
Gurjit Kaur
The present need |
For Mothers-to-be
n Ask your doctor about availability of prenatal screening tests for chromosomal aneuploidies and neural tube defects and the right time to get them done.
n Or, on the recommendation of your doctor, you can get enrolled under the ongoing prenatal screening programme at Genetic Centre, GMCH. For Health Professionals n Prenatal Screening tests for chromosomal aneuploidies and neural tube defects are as important as any other examination during pregnancy. Be informed about the importance and the significance of these tests, their availability in your area and the right timings of these tests.
n Explain the need of getting these tests done to your patients and get these tests done at the appropriate time keeping in consideration the period of legal medical termination of pregnancy in India.
n Prenatal screening is not mere biomarker testing but is a complete programme encompassing testing, correct interpretation of results, ultrasound evaluation, confirmatory tests and counselling to patient at all levels of testing.
n Different sets of soft-markers are evaluated in first and second trimester of pregnancy.
n Update yourself with latest soft-markers associated with a risk of carrying a fetus with chromosomal
aneuploidies. For Families with Previous Down's baby n Having one baby affected with DS does not mean that other pregnancies would also be affected. For further pregnancies, go for prenatal screening for chromosomal
aneuploidies.
n Get in touch with societies working for the betterment of DS children. Genetic Centre at Government Medical College and Hospital, Chandigarh, along with Genetic Unit, All India Institute of Medical Sciences (AIIMS) and Genetic Unit, Maulana Azad Medical College, is very soon going to launch a society for Down Syndrome for the betterment of DS children. For Government n Recognise the significance of prevention-based screening and bring it into focus of maternal and child health care.
n Introduce prenatal screening facilities as pilot studies at different centres in India.
n Institute programmes promoting awareness among general public and in the long run make such preventive screening programmes mandatory for all. |

With the support of Chandigarh Administration, at Genetic Centre, Government Medical College and Hospital, Sector 32,
Chandigarh, prenatal screening tests are available under the Prenatal Screening Programme to all pregnant women at nominal rates. Any pregnant women can get herself enrolled and screened for these fetal aneuploidies at Genetic
Centre, GMCH with the recommendation and referral from her obstetrician. The American College of Obstetricians and Gynecologists
(ACOG) recommends that DS screening test must be offered to all pregnant women regardless of age or prior history.
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Mental
retardation, the commonest form of developmental disability, is a condition in which there is delay or deficiency in all aspects of development, i.e. there is global and noticeable deficiency in the development of motor, cognitive, social, and language functions. It affects about 1-3 per cent of the population. There are many causes of mental retardation, but doctors are able to find a specific reason in only 25 per cent of cases. Ignorance about the causes of mental retardation and social stigma and discrimination generally observed among people add to the suffering attached with it. Mental retardation, the commonest form of developmental disability, is a condition in which there is delay or deficiency in all aspects of development, i.e. there is global and noticeable deficiency in the development of motor, cognitive, social, and language functions. It affects about 1-3 per cent of the population. There are many causes of mental retardation, but doctors are able to find a specific reason in only 25 per cent of cases. Ignorance about the causes of mental retardation and social stigma and discrimination generally observed among people add to the suffering attached with it. Chromosomal abnormalities are one of the leading cause of mental retardation and physical handicap. Most chromosomal abnormalities are due to an extra copy of a particular chromosome. Other causes may be chromosome breakage or arrangement in a wrong order. Abnormal chromosomes are caused by defective development of sperm or egg cells. It is difficult to pinpoint the exact nature of the cause but one thing is for sure. There is no cure for chromosomal abnormalities and for those suffering from such disorders life-long management is required.
AbnormalitiesAbout 70 per cent miscarriages in early pregnancy are thought to be the results of chromosomal abnormalities. In some chromosomal abnormalities, the fetus survives and grows up as an individual. Down's syndrome (DS), the most common cause of birth defects, is one such abnormality in which the fetus survives during pregnancy. It is a genetic condition in which a person has 47 chromosomes instead of 46. The presence of extra chromosome is referred to as trisomy. In about 95 per cent of cases of Down's syndrome there is an extra copy of chromosome 21 and hence, Down syndrome is often known as Trisomy 21. This extra chromosome causes problems with the way the body and brain develop. Trisomy 21 presents with a wide range of mental retardation. Several other effects associated with DS include mild to severe developmental delay, heart defects, epilepsy, respiratory problems, susceptibility to infection, celiac diseases, Alzheimer's etc. Throughout the world the overall prevalence of DS is 10 per 10,000 live births. DS symptoms vary from person to person and can range from mild to severe. However, children with DS have widely recognised characteristic appearance i.e. head smaller than normal, inner cornea of eye may be rounded, small mouth, wide short hands with short fingers. Physical, mental and social development may also be delayed in children. Advancing maternal age, having had one child with DS and being carriers of the genetic translocation for DS are some risk factors which increase the risk of having a DS baby. With the advancement of science and technology it is possible to detect these birth defects during the development of fetus i.e. during pregnancy. This is done worldwide through Prenatal Screening Programme.
BiomarkersDuring the development of fetus there are certain biomarkers produced in the fetus which pass through the placenta and enter into the mother's blood stream. Biomarkers are proteins or hormones secreted by growing fetal parts which pass via amniotic fluid and placenta and enter into the maternal circulation. These include AFP (alpha-fetoprotein), HCG (human chorionic gonadotropin), UE3 (Unconjugated estriol) and PAPP-A (Pregnancy Associated Plasma Protein A). These biomarkers can be measured in the mother's blood during the development of the fetus. Under normal conditions there is a specific pattern of increase or decrease of these biomarkers with the gestational age. Any deviation from this specific pattern helps to recognise pregnancies at higher risk of certain abnormalities. These biomarkers are tested twice during pregnancy i.e. between 9th and 13th week (first trimester) and between 15th and 19th week (second trimester). The test for first trimester is called Dual test and for second trimester is called Triple test. The objective of screening is to segregate the test population into a low-risk group and a high-risk group. Once the baby with DS is born then throughout life the child has to be managed. There is no treatment for total cure or eliminating DS, as it a birth defect. which means that the basic unit i.e. the cells of the body have abnormal number of chromosomes, which cannot be changed. Through prenatal screening we can detect such birth defects during development of the fetus and through genetic counselling we can help the parents understand the disorder and its life-long management. The parents can further decide whether they want to continue the pregnancy or opt for medical termination. One important issue which I would like to highlight is that as per Indian law the medical termination is possible only before the 20th week of pregnancy. Hence, screening and confirmatory tests should be carried out as early as possible and before the 20th week of pregnancy, so that the parents can make an informed choice.
Various factorsPrenatal screening test and calculations depends upon various factors like:-
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Sensitivity of test
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Cut-off values for the population being tested
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Period of Gestation It should be remembered that screening test is different from a confirmatory test. In a screening test we divide the population into low-risk group and a high-risk group, whereas a confirmed diagnosis is obtained in case of a confirmatory test. Low-risk means that chance of the occurrence of a disease is low, while high risk commands further testing to be sure that the fetus is normal. Further testing includes advanced ultrasonography, invasive testing like chorionic villus sampling or amniocentesis. In an advanced ultrasound we look for various softmarkers which are associated with congenital abnormalities and through invasive testing chromosomal number and structure are examined. It is important to note that all the testing procedures under prenatal screening must be completed within 20 weeks of pregnancy since, as per Indian law, medical termination cannot be carried out after this period.
CounsellingCounselling to patients called Genetic counselling is another integral part of prenatal screening programmes. It is a continuous process where counselling is provided to all enrolled couples prior to their enrollment into the screening programme and at all stages of progress of prenatal screening to facilitate thorough understanding of the objective and process of screening procedure and the necessity of carrying out any additional testing. All tests are voluntary and informed consent is taken prior to testing. There is an urgent need of our doctors to be aware of prenatal screening programme, its importance and necessity in today's time. It should be known that prenatal screening is not just one single test. It is a complete programme where testing, interpretation of results, ultrasound evaluation, confirmatory tests and genetic counselling must be provided. Maternal and child health forms the backbone of the concept of healthy family and an essential part of the reproductive health package. Prenatal screening already forms an integral part of healthcare in all developed countries. Owing to their prevention-based approach, the mass screening programmes gain significantly over traditional treatment-based management. However, screening-for-all has shown little development in India except in very few selected centres in metropolitan cities and chiefly as private setups. India has a high birth rate and hence a very large number of infants with genetic disorders are born every year. The available data point out that in India approximately 30,000 Down syndrome babies are born annually. Once a child with DS is born, then only management is available. The responsibility of the child throughout life rests with the family of the child. There are no insurance policies in India to take care of the medical needs of the child and provide financial support. Parents often have to take the child to hospital from time to time for treatment of various defects associated with it. A handicapped child is not only a drain on the financial resources of the family but it is also extremely emotionally exhausting for the family members. Thus, physical and mental handicap in a member of the family exerts pressure on the limited resources of the family, society and the country and overall presents itself as a socio-economic burden. However, preventive screening which is an integral part of health care throughout the world offers early information about genetic disorders in the fetus. Prenatal Screening for chromosomal disorders is available since 20th century in developed countries but, unfortunately, Indian health care policymakers have not yet even considered introducing an existing preventive health care facility in our country. The magnitude of numbers and the suffering, social stigma and economic burden that these disorders exert should shake us from our deep slumber of insensitivity and inspire health policy makers to bring into focus preventive health care facilities in our country along with the existing health care programmes. Public health authorities need to organise genetic services in a comprehensive and integrated manner and promote awareness and availability of facilities so as to improve the standard of antenatal care. The success encountered by the government of India in its efforts to control communicable diseases, especially Pulse Polio Immunisation Programme can be easily replicated in case of genetic disorders if the government brings prevention-based screening into its direct focus for improving maternal and child health care. The writer is Consultant Incharge, Genetic Centre; Assoc Professor, Physiology, Government Medical College and Hospital, Chandigarh
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