Abu Dhabi: 3-year-old Emirati boy finds new hope after neurological treatment

A three-year-old Emirati boy, who faced difficulties in standing and walking due to a rare neurological disease, has been given a new hope following a new treatment by Abu Dhabi doctors.

Abu Dhabi Health Services Company (Seha) says it has used a new genetic therapy to successfully treat the Emirati boy suffering from Duchenne Muscular Dystrophy (DMD).

With the child facing difficulties with standing and walking, the parents brought the child to Seha’s Sheikh Shakhbout Medical City (SSMC) for a diagnosis.

After a series of comprehensive tests, doctors diagnosed him with DMD, a rapidly progressive form of muscular dystrophy. With the diagnosis, the child was referred to Sheikh Khalifa Medical City (SKMC), a SEHA healthcare facility, to access life-changing treatment.

DMD is a genetic disorder that causes progressive skeletal muscular weakness in children. If left without proper treatment, it can progress to affect the cardiac muscles and cause children to lose their ability to walk and develop scoliosis. This disease can also shorten the child’s life expectancy.

The new therapy - Amondys 45 - was provided for the first time in the UAE at SKMC to treat the child after being diagnosed with DMD.

Dr Omar Ismayl, Consultant Paediatric Neurologist at SKMC, said: “Thanks to the new therapy treatments available at SKMC, such as Amondys 45, we are able to give the child and his parents new hope. This particular medication, administered as an intravenous infusion, allows for the production of the functional form of dystrophin: the protein that plays a vital role in maintaining muscle strength and is dysfunctional in children with DMD. This is a much-needed breakthrough and will enhance quality of life for many children living with DMD.”

Dr Ismayl added: “Thirty percent of children who are affected with DMD are reported as the first sufferers in their families, while 70 percent are hereditary with previous cases in relatives, especially from the mother’s side. This neurological condition is caused by abnormal mutations or deletion in the dystrophin gene, which produces the essential protein that allows muscles to continue to be healthy and functioning.

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