Anti-tumour necrosis factor treatment for the prevention of ischaemic events in patients with deficiency of adenosine deaminase 2 (DADA2)

S Cooray, E Omyinmi, Y Hong, C Papadopoulou… - …, 2021 - academic.oup.com
Objective To evaluate the impact of anti-Tumour Necrosis Factor-α (anti-TNF) treatment on
the occurrence of vasculitic ischaemic events in patients with deficiency of adenosine …

The many faces of a monogenic autoinflammatory disease: adenosine deaminase 2 deficiency

JL Kendall, JM Springer - Current Rheumatology Reports, 2020 - Springer
Abstract Purpose of Review We aim to describe the pathophysiology, clinical findings,
diagnosis, and treatment of deficiency of adenosine deaminase 2 (DADA2). Recent Findings …

Deficiency of adenosine deaminase 2 in adults and children: experience from India

A Sharma, G Naidu, V Sharma, S Jha… - Arthritis & …, 2021 - Wiley Online Library
Objective Deficiency of adenosine deaminase 2 (DADA2) is a potentially fatal monogenic
syndrome characterized by variable manifestations of systemic vasculitis, bone marrow …

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study

R Caorsi, F Penco, A Grossi, A Insalaco… - Annals of the …, 2017 - ard.bmj.com
Objectives To analyse the prevalence of CECR1 mutations in patients diagnosed with early
onset livedo reticularis and/or haemorrhagic/ischaemic strokes in the context of inflammation …

A monogenic disease with a variety of phenotypes: deficiency of adenosine deaminase 2

S Özen, ED Batu, EZ Taşkıran, HA Özkara… - The Journal of …, 2020 - jrheum.org
Objective. Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive
autoinflammatory disorder associated with ADA2 mutations. We aimed to investigate the …

DADA2 diagnosed in adulthood versus childhood: a comparative study on 306 patients including a systematic literature review and 12 French cases

A Fayand, F Chasset, D Boutboul, V Queyrel… - Seminars in Arthritis and …, 2021 - Elsevier
Background Deficiency of adenosine deaminase 2 (DADA2) is a rare autoinflammatory
disease usually presenting before the age of 10 years. Non-specific clinical features or late …

Identification of novel adenosine deaminase 2 gene variants and varied clinical phenotype in pediatric vasculitis

KM Gibson, KA Morishita, P Dancey… - Arthritis & …, 2019 - Wiley Online Library
Objective Individuals with deficiency of adenosine deaminase 2 (DADA 2), a recently
recognized autosomal recessive disease, present with various systemic vascular and …

Screening of 181 patients with antibody deficiency for deficiency of adenosine deaminase 2 sheds new light on the disease in adulthood

J Schepp, M Proietti, N Frede, M Buchta… - Arthritis & …, 2017 - Wiley Online Library
Objective We aimed to test the relevance of deficiency of adenosine deaminase 2 (DADA2)
in patients with antibody deficiency and describe the clinical picture of the disease in …

Clinical, imaging and genotypical features of three deceased and five surviving cases with ADA2 deficiency

S Sahin, A Adrovic, K Barut, S Ugurlu… - Rheumatology …, 2018 - Springer
Deficiency of adenosine deaminase type 2 (DADA2) is a rare form of autoinflammatory
disorder with limited reported cases. In this paper, we have presented the clinico …

A case series of adenosine deaminase 2-deficient patients emphasizing treatment and genotype-phenotype correlations

ED Batu, O Karadag, EZ Taskiran, U Kalyoncu… - The Journal of …, 2015 - jrheum.org
There are a number of original features in this series. To our knowledge, this is the first
report of DADA2 patients developing progressive and debilitating renal findings (FSGS …