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Youngest Child In Dammam Begins Life-Saving Dialysis Treatment
This case represents a significant milestone in the Eastern Province, as it is the first instance of dialysis treatment for a child of such low weight. It underscores the hospital’s dedication to providing specialized and compassionate care for young patients facing complex medical challenges.
The hospital confirmed that the child was admitted with chronic kidney failure due to a rare genetic condition known as Primary Hyperoxaluria Type 1 (PH1). This condition causes the body to produce excessive amounts of oxalate, which can lead to kidney damage. The medical team successfully inserted a permanent dialysis catheter, enabling the child to receive the first dialysis treatment of its kind at the hospital, a vital step in managing this challenging health issue.
These deposits can lead to kidney failure and may also accumulate in other areas of the body, including the bones, which can result in additional complications. Intensive dialysis is essential to reduce oxalate levels in the blood, making this case particularly significant in the Eastern Province, especially given the child’s low weight of only 7 kg. Daily treatments will be critical in effectively managing this rare condition.
The hospital has successfully handled this unique situation through specialized equipment tailored for children. The medical team comprises experienced professionals trained in pediatric dialysis, all committed to delivering the highest standard of care. Their expertise, along with the availability of advanced technology, ensures that the child receives optimal treatment in a safe and supportive environment.
Minimum custom amount to enter is AED 2
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