Primary hyperoxaluria type 1 in children: clinical and laboratory manifestations and outcome.
Hala WannousPublished in: Pediatric nephrology (Berlin, Germany) (2023)
PH1 is still a grave disease with wide variety of clinical presentations which frequent results in delays in diagnosis, thus kidney failure is still a common presentation. In Syria, we face many challenges in diagnosis of PH, especially PH2 and PH3, and in management, with hopes that diagnosis tools and modern therapies will become available in our country. Graphical abstract A higher resolution version of the Graphical abstract is available as Supplementary information.
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