ArticleJournal of community genetics2015
Pakistani mothers' and fathers' experiences and understandings of the diagnosis of Down syndrome for their child.
Article in Journal of community genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Experiences of caregivers and healthcare providers regarding health services for children with Down syndrome in Karachi; Pakistan.PLOS global public health · 2026Article
- Whispers of Resilience: A phenomenological exploration of maternal journeys with children affected by Downs Syndrome in Quetta, Baluchistan.Pakistan journal of medical sciences · 2025Article
- Down syndrome: Parental experiences of a postnatal diagnosis.Journal of intellectual disabilities : JOID · 2023Review
- Attitudes of Filipino parents of children with Down syndrome on noninvasive prenatal testing.Journal of community genetics · 2022Article
- Assessing Health-Related Quality of Life, Morbidity, and Survival Status for Individuals With Down Syndrome in Pakistan (DS-Pak): Protocol for a Web-Based Collaborative Registry.JMIR research protocols · 2021Article
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Authors and funding
5 authors.
Funding
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Abstract
Down syndrome (DS) is a relatively common chromosomal condition, which can be diagnosed prenatally. However, little is known about the diagnosis of the condition in developing countries. This qualitative study explored parents' experiences of the diagnosis of DS in Pakistan. Fifteen mothers and fifteen fathers of children with DS had semi-structured interviews, which were analysed using thematic analysis. All the parents received their child's diagnosis after birth, ranging from the postnatal period to 7 years of age. Parents recalled receiving little or no information at the time of diagnosis, leading to misunderstandings about the cause and nature of their child's condition. Some parents referred to their child being "Mongol" and were unaware of "Down syndrome" as the more appropriate term for the condition. Use of such terms for DS restricted parents' ability to source further information about the condition. Many parents showed poor understanding of the aetiology and prognosis of the condition. Improved training for healthcare professionals in recognising key features of DS in the neonatal period or in early childhood could enable earlier diagnosis of the condition. In addition, provision of accurate information in a sensitive manner following diagnosis could enable parents to optimise their child's well-being.
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