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Figures obtained by The Mail on Sunday under Freedom of Information laws reveal a huge challenge, not only for such communities, but also for the Health Service. The figures show that up to 20 per cent of the children treated for congenital problems in cities such as Sheffield, Glasgow and Birmingham are of Pakistani descent, a figure significantly greater than the background populations, which can be four per cent or lower.
Birmingham Children’s Hospital alone has seen the number of Pakistani children treated for genetic disorders increase by as much as 43 per cent since 2011.
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Her twin brother Ahmed died aged just two-and- a-half.
Her elder sister Tahira has serious learning difficulties, and another brother, Kasim, born just two years after Sarfraz’s death, had problems so severe that he required 24-hour care and did not live to see his 18th birthday. Yet the real tragedy is not only that their experience is far from rare, but that it could have been avoided.
Aisha’s Pakistani-born parents, Mohammed and Barkat, are first cousins.
There is fresh and growing evidence that marriage between relatives within the Pakistani community may be to blame – in part at least – for a dramatic rise in the number of children with genetic disorders being treated in British hospitals.
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