Literature DB >> 22258353

β-Thalassemia in Pakistan: a pilot program on prenatal diagnosis in Multan.

Shahid Mahmood Baig1, Dure Sabih, Muhammad Kashif Rahim, Aysha Azhar, Muhammad Tariq, Muhammad Sajid Hussain, Syed Muhammad Saqlan Naqvi, Ghazala Kaukab Raja, Tahir Naeem Khan, Muhammad Jameel, Zahra Iram, Samia Noor, Usman Raza Baig, Javed Anver Qureshi, Shehla Anjum Baig, Syeda Marriam Bakhtiar.   

Abstract

Prenatal diagnosis (PND) of β-thalassemia has been underutilized in Pakistan because of a number of social and economic factors. National Institute for Biotechnology and Genetic Engineering Faisalabad in collaboration with Multan Institute of Nuclear Medicine and Radiotherapy Multan introduced free PND service for carrier couples of Multan district. Multan has a population of about 4 million. More than 170 couples registered for retrospective PND and in 2 years 105 PND were carried out through first trimester chorionic villus sampling. Almost 90% of these couples were unable to afford the cost of PND and would not have undergone the test as free service was not available. Monoplex and Multiplex Amplification Refractory Mutation System-polymerase chain reaction and genomic DNA sequencing were used for detection of IVS (intervening sequence)-I-5 (G-C), FSC (frameshift codon)-8/9 (+G), FSC-41/42 (-TTCT), IVS-I-1 (G-T), 619 bp deletion, and CD-15 (G-A) β-globin mutations. Eighty-one percent (85/105) couples analyzed were in a consanguineous marriage. Twenty-three fetuses were found homozygous mutant and all couples opted for discontinuation of affected pregnancies. More families are registering for PND after establishment of this free and accessible PND service.

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Year:  2012        PMID: 22258353     DOI: 10.1097/MPH.0b013e31823752f3

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  4 in total

1.  NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes.

Authors:  Ayaz Khan; Shixiong Tian; Muhammad Tariq; Sheraz Khan; Muhammad Safeer; Naimat Ullah; Nazia Akbar; Iram Javed; Mahnoor Asif; Ilyas Ahmad; Shahid Ullah; Humayoon Shafique Satti; Raees Khan; Muhammad Naeem; Mahwish Ali; John Rendu; Julien Fauré; Klaus Dieterich; Xenia Latypova; Shahid Mahmood Baig; Naveed Altaf Malik; Feng Zhang; Tahir Naeem Khan; Chunyu Liu
Journal:  Mol Genet Genomics       Date:  2022-08-24       Impact factor: 2.980

2.  The views of Pakistani doctors regarding genetic counseling services - is there a future?

Authors:  Myla Ashfaq; Farhana Amanullah; Ayesha Ashfaq; Kelly E Ormond
Journal:  J Genet Couns       Date:  2013-03-29       Impact factor: 2.537

3.  Knowledge and Beliefs Regarding Thalassemia in an Urban Population.

Authors:  Sidra Ebrahim; Anum Z Raza; Mahnoor Hussain; Arsalan Khan; Lavita Kumari; Ramsha Rasheed; Saad Mahmood; Muneeza A Khatri; Manaal Bijoora; Ramsha Zaheer; Naveed Sattar; Wafa Sohail; Hareem Zakir; Fatima H Jafry; Areeba Memon; Shayan Anwer; Kaneez Fatima
Journal:  Cureus       Date:  2019-07-29

4.  Enabling routine β-thalassemia Prevention and Patient Management by scalable, combined Thalassemia and Hemochromatosis Mutation Analysis.

Authors:  Ghazala Hashmi; Asim Qidwai; Kristopher Fernandez; Michael Seul
Journal:  BMC Med Genet       Date:  2020-05-15       Impact factor: 2.103

  4 in total

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