𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Prenatal diagnosis of β-thalassaemia and other haemoglobinopathies in India

✍ Scribed by Chitra Thakur (Mahadik); Flavian Vaz; Monisha Banerjee; Chhaya Kapadia; P. G. Natrajan; Harsha Yagnik; Sudha Gangal


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
115 KB
Volume
20
Category
Article
ISSN
0197-3851

No coin nor oath required. For personal study only.

✦ Synopsis


This paper reports prenatal diagnosis of 787 fetuses of b-thalassaemia and other haemoglobinopathies in Indian high-risk communities. DNA based diagnosis was offered in the ®rst, as well as the second trimester, in 489 pregnancies (with ®ve twins) on fetal tissues such as chorionic villus (CV) and amniocytes using the ampli®cation refractory mutation system (ARMS) and restriction fragment length polymorphism (RFLP) techniques. Two hundred and ninety-two women (with one twin), who either presented late in the second trimester or whose DNA diagnosis was not informative, were offered prenatal diagnosis using globin chain synthesis (GCS) on fetal blood cells. Maternal contamination of fetal DNA was ruled out by variable number tandem repeat (VNTR) analysis using sites in four different genes (Apo-B, D1S-80, Ig-JH and Haras), while contamination of fetal blood was checked by a particle size distribution channelyzer. Using both techniques we were able to offer complete diagnosis in 99.8% cases. Out of 494 fetuses tested by DNA analysis, 135 were found to be normal, 201 were carriers, whereas 146 were affected. Out of 293 fetuses analysed by GCS, 215 were unaffected and 71 were affected. In this study, both fetuses were tested in twin pregnancies, of which three required selective termination of one fetus. Because of social, religious taboos and family in¯uences, genetic counselling was found to be an important guideline for couples selecting options for prenatal diagnosis. Our experience suggests that because of late presentation by many couples to the diagnostic centres, in developing countries like India, both the techniques of DNA analysis and GCS should be made available at major referral centres for maximum bene®t to couples.


📜 SIMILAR VOLUMES


Fetal nuchal translucency and prenatal d
✍ Giovanni Monni; Rosa M. Ibba; Maria A. Zoppi; Monica Putzolu; Marcella Floris; A 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 134 KB

In Sardinia, fetal karyotyping for couples at risk for -thalassaemia is offered only to women \_35 years and for specific risk of chromosomopathies. This policy is not easily accepted by the couples who insistently request additional karyotyping. In order to select those at highest risk of chromosom

Prenatal diagnosis of β-thalassaemia: ex
✍ Renu Saxena; Pawan K. Jain; Elizabeth Thomas; Ishwar C. Verma 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 75 KB 👁 1 views

We present our experience with the amplification refractory mutation system (ARMS) for the prenatal diagnosis of -thalassaemia in 415 pregnancies of 360 women. Five mutations of the -thalassaemia gene common in Asian Indians accounted for 89•2 per cent and rare mutations for 7•2 per cent of all muta

Prenatal diagnosis of β-thalassaemia by
✍ Pranee Winichagoon; Vannarat Saechan; Roongrat Sripanich; Chamnong Nopparatana; 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 240 KB

Thalassaemia is the most common genetic disease and is a public health problem of Thailand. Prevention and control of -thalassaemia diseases need accurate diagnosis of carriers and proper genetic counselling. Prenatal diagnosis is needed to prevent birth of the thalassaemic offspring in the couple a

Rapid Mid-Trimester Prenatal Diagnosis o
✍ V. B. Rao; P. G. Natrajan; C. P. Lulla; S. B. Bandodkar 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 97 KB 👁 2 views

Anion exchange high performance liquid chromatography (AX-HPLC) has been widely used for separating and quantifying various haemoglobin fractions especially in the haemoglobinopathies. We have evaluated the reliability of this technique to measure low concentrations of adult haemoglobin (HbA) in fet

ACCEPTANCE OF FIRST-TRIMESTER PRENATAL D
✍ L. ZAHED; J. BOU-DAMES 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 196 KB 👁 1 views

We have interviewed 83 couples at risk for a haemoglobin disorder, mostly -thalassaemia, in an effort to evaluate their attitude towards first-trimester prenatal diagnosis. Most of the families had received poor education and were of low socio-economic status and more than half of the couples were n

Prenatal diagnosis of beta-thalassaemia
✍ Suhaib Ahmed; Mohammad Saleem; Nadra Sultana; Yasmeen Raashid; Amin Waqar; Masoo 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 94 KB 👁 1 views

A service for prenatal diagnosis of beta-thalassaemia was introduced in Pakistan in May 1994. Two renowned Islamic scholars, consulted before the service was introduced, ruled that a pregnancy can be terminated if the fetus is affected by a serious genetic disorder, and if termination is before 120