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Newborn screening in Pakistan - lessons from a hospital-based congenital hypothyroidism screening programme
Bushra Afroze1, Khadija Nuzhat Humayun, Maqbool Qadir
1Department of Paediatrics and Child Health. The Aga Khan University Hospital Karachi, Stadium Road, PO Box 3500, Karachi 74800, Pakistan. bushraahasan@yahoo.com
Insights
Newborn screening for congenital hypothyroidism in Pakistan is crucial despite infrastructure challenges. An estimated incidence of 1 in 1600 live births highlights the need for a national program.
Area of Science:
- Medical Genetics
- Public Health
- Neonatal Care
Background:
- Biotechnology, particularly involving human subjects, presents complex ethical, legal, social, and religious issues.
- Establishing newborn screening programs in developing countries faces challenges competing with other health priorities.
- Newborn screening saves lives and prevents serious complications, making it imperative for developing nations.
Purpose of the Study:
- To highlight the importance of newborn screening programs in developing countries.
- To assess the feasibility and challenges of implementing newborn screening in Pakistan.
- To estimate the incidence of congenital hypothyroidism in Pakistan.
Main Methods:
- A 20-year audit of congenital hypothyroidism screening at Aga Khan University Hospital (AKUH).
- Detailed review of data over 10 months in 2008 for repeat thyroid stimulating hormone (TSH) testing.
- Calculation of estimated incidence of congenital hypothyroidism (CH).
Main Results:
- Aga Khan University Hospital (AKUH) and other local hospitals conduct newborn screening for congenital hypothyroidism.
- The primary barrier to implementation is Pakistan's inadequate health infrastructure, with 80% of deliveries occurring at home.
- An estimated incidence of 1 in 1600 live births for congenital hypothyroidism was found during a 10-month period in 2008.
Conclusions:
- Despite challenges, newborn screening is vital for preventing infant mortality and morbidity.
- Pakistan lacks a national newborn screening program, with limited genetic and metabolic services available.
- Further efforts are needed to establish robust newborn screening infrastructure and services in Pakistan.
Abstract:
We are living in a time of unprecedented increase in knowledge and rapidly changing technology. Such biotechnology especially when it involves human subjects raises complex ethical, legal, social and religious issues. The establishment of newborn screening programmes in developing countries poses major challenges as it competes with other health priorities like control of infectious diseases, malnutrition and immunization programmes. Despite this, it is imperative that the importance of newborn screening programmes is recognised by developing countries as it has been proven through decades of experience that it saves thousands of babies from mental retardation, death and other serious complications. Pakistan has an estimated population of 167 million inhabitants, 38.3% of whom are under 15 years of age. Pakistan lacks a national programme for newborn screening. However, as individual practice at the local level, Aga Khan University Hospital (AKUH) and a few other hospitals are doing newborn screening for congenital hypothyroidism. The main hurdle in the implementation of newborn screening in Pakistan is the lack of good infrastructure for health. Eighty percent of deliveries take place at home. Moreover, little resources are available for children identified with a genetic condition due to the non-existence of genetic and metabolic services in Pakistan. In a 20-year audit of congenital hypothyroid screening at AKUH we found 10 babies with congenital hypothyroidism. However due to missing data links spanning several years, we were unable to calculate its true incidence during this period. In order to estimate the incidence of congenital hypothyroidism (CH) we reviewed in detail data over 10 months in 2008, a period where there was better compliance for repeat thyroid stimulating hormone (TSH) testing, and found 2 babies with CH. This gave an estimated incidence of 1 in 1600 live births.
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