A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-α

Sezgin SahinDepartment of Paediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, TurkeyCorrespondence[email protected]
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Amra AdrovicDepartment of Paediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey

Kenan BarutDepartment of Paediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey

Selen BaranDepartment of Paediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey

Eda Tahir TuranliDepartment of Molecular Biology and Genetics, Faculty of Science and Letters, Istanbul Technical University, Istanbul, Turkey

Nur CanpolatDepartment of Paediatric Nephrology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey

Osman KizilkilicDivision of Neuroradiology, Department of Radiology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey

Ozan OzkayaDepartment of Paediatrics, Okmeydanı Research Hospital, Istanbul, Turkey

Ozgur KasapcopurDepartment of Paediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey

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