{"id":14272,"date":"2024-10-15T10:45:48","date_gmt":"2024-10-15T10:45:48","guid":{"rendered":"https:\/\/news.godj.com\/news\/girls-life-saved-by-pioneering-study-of-rare-diseases\/"},"modified":"2024-10-15T10:45:48","modified_gmt":"2024-10-15T10:45:48","slug":"girls-life-saved-by-pioneering-study-of-rare-diseases","status":"publish","type":"post","link":"https:\/\/news.godj.com\/news\/girls-life-saved-by-pioneering-study-of-rare-diseases\/","title":{"rendered":"Girl\u2019s life saved by pioneering study of rare diseases"},"content":{"rendered":"


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\"LisaLisa Hawker<\/span><\/div>\n<\/div>\n<\/figure>\n
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The family of a young girl say her life was saved after a pioneering study was able to diagnose her incredibly rare genetic disorder, leading to better treatment.<\/p>\n

Jaydi Hawker, 11, has a form of dwarfism thought to affect fewer than 50 people in the world.<\/p>\n

There are thousands of such genetic disorders and, collectively, they affect one in 17 people in the UK.<\/p>\n

Jaydi was part of a study pushing the limits of genetic analysis to get families a diagnosis.<\/p>\n<\/div>\n

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The disorders are caused by mutations in our DNA, which damage crucial instructions for how our bodies should work. <\/p>\n

Parents and doctors will spot something wrong with a child\u2019s development but discovering the cause – the specific mutation in our entire genetic code – is often elusive.<\/p>\n

Jaydi\u2019s mum Lisa Hawker says she first knew something was wrong when a pregnancy anomaly scan highlighted unusual brain development.<\/p>\n

Jaydi was born at 31 weeks, weighing just 2lbs (0.9kg) and continued to grow and develop slowly.<\/p>\n

\u201cShe was so tiny, smaller than a doll, even dolls’ clothes were too big,\u201d says the single mum from Seaton, in Devon.<\/p>\n

Jaydi left hospital only a week before her first birthday.<\/p>\n<\/div>\n

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\"LisaLisa Hawker<\/span><\/div>\n<\/div>\n

Jaydi was fed via a nasogastric tube to provide food and liquid into her stomach<\/figcaption><\/p>\n<\/figure>\n
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“She just wasn\u2019t putting on weight despite having tube feeds, extra calories, and also her development was delayed and we just didn\u2019t know what was going on,” says Dr Emma Kivuva, clinical geneticist at the Royal Devon University Healthcare NHS Foundation Trust.<\/p>\n

A genetic disorder was suspected but no amount of testing confirmed it.<\/p>\n

Lisa says: \u201cIt was not knowing why she wasn\u2019t growing, why her head was so little.<\/p>\n

\u201cIt was really stressful, I blamed myself, did I do something wrong? Did I not eat enough or drink enough or wait too long in life? And just driving yourself crazy not knowing.\u201d<\/p>\n<\/div>\n

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When Jaydi was nearly one, Dr Kivuva offered a place on the Deciphering Developmental Disorders study. <\/p>\n

The largest ever study of children with genetic disorders, it is a collaboration between the NHS, universities and the Sanger Institute, which specialises in analysing DNA.<\/p>\n

Years later it would provide answers but initially Lisa and Jaydi had to navigate the uncertainties of an unknown condition. <\/p>\n

\u201cShe\u2019d been in hospital for so long she didn\u2019t even know I was her mum, she\u2019d been handled by so many nurses for so long,” says Lisa, who even tried playing hospital sounds to soothe her daughter.<\/p>\n

Jaydi learned to walk and started nursery but she is non-verbal and has problems seeing and hearing.<\/p>\n

Lisa says at one point “the whole side of her face had collapsed” and doctors thought she would need major reconstructive surgery to relieve pressure on her brain. Blood and bone marrow tests showed Jaydi’s blood was thin like water.<\/p>\n

\u201cEvery day was like living with a ticking timebomb,\u201d says Lisa.<\/p>\n<\/div>\n

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\"LisaLisa Hawker<\/span><\/div>\n<\/div>\n<\/figure>\n
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Answers came when Jaydi was four years old.<\/p>\n

The detailed analysis of her DNA found she had lig-4 syndrome. It is caused by a mutation that affects the body\u2019s ability to repair DNA damage and had only been documented a handful of times before.<\/p>\n

\u201cThe penny dropped, it all made sense,\u201d says Lisa.<\/p>\n

The diagnosis connected the primordial dwarfism, the development delays and what was happening in her blood.<\/p>\n

For Lisa, the diagnosis ended years of searching for an answer. For clinicians, it meant they could compare Jaydi\u2019s notes with other cases of lig4 from around the world. <\/p>\n

\u201cAs doctors, particularly at a time we were trying to understand her bone marrow tests, it meant we had an explanation and knew what to do about it,\u201d said Dr Kivuva.<\/p>\n

Children with lig-4 syndrome were at an increased risk of aggressive and hard to treat leukaemia.<\/p>\n

Rather than wait for that to happen, Lisa and doctors agreed an immediate bone marrow transplant could save Jaydi’s life. <\/p>\n

It involved Jaydi and Lisa staying in a sterile room for six months because of the risk of infection but Lisa says it was worth it.<\/p>\n

She says: “The bloods are all back to normal, she\u2019s back to school, she\u2019s running round like a crazy child and she\u2019s really happy and healthy at the moment.<\/p>\n

“I think if we hadn\u2019t got that diagnosis it would have been too late\u2026 it saved Jaydi\u2019s life.”<\/p>\n

She says Jaydi is full of energy, loves singing and dancing and is currently going through a fake nails phase.<\/p>\n<\/div>\n

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\"LisaLisa Hawker<\/span><\/div>\n<\/div>\n<\/figure>\n
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Lisa and Jaydi are among 13,500 families that have taken part in the Deciphering Developmental Disorders study.<\/p>\n

Previous analysis showed it identified 60 new genetic diseases and gave 5,500 families a diagnosis for the first time.<\/p>\n<\/div>\n

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The latest study, led by the University of Exeter and the Royal Devon University Healthcare NHS Foundation Trust, looked at whether getting a diagnosis made a difference.<\/p>\n

The results, published in the journal Genetics in Medicine Open<\/a>, found:<\/p>\n