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Any disease or disorder in which the cause of the disease is a mutation in the ADA2 gene.
No HPO annotations are available for this condition.
Deficiency of adenosine deaminase 2 (DADA2) is a systemic autoinflammatory disorder in which the three major manifestations are vasculitis, dysregulation of immune function, and hematologic disease . Other clinical features include neurologic, gastrointestinal, and musculoskeletal involvement. Severe manifestations (e.g., strokes or ischemic injuries to tissues and/or organs) can cause disability and/or be life threatening. Prior to the discovery of the molecular pathogenesis of DADA2 and adequate therapies, death before age 30 years was reported in 8% of affected individuals .
Formal diagnostic criteria for adenosine deaminase 2 deficiency (DADA2) have not been established.
Adenosine deaminase 2 deficiency (DADA2) should be suspected in individuals with clinical and laboratory findings of systemic autoinflammatory disease characterized by vasculitis, dysregulation of immune function, and hematologic abnormalities .
Systemic Autoinflammatory Disease
Clinical findings
No approved treatments are currently available for deficiency of adenosine deaminase 2. The disease remains an area of unmet medical need.
To establish the extent of disease and needs in an individual diagnosed with adenosine deaminase 2 deficiency (DADA2), the evaluations summarized in this section (if not performed as part of the evaluation that led to the diagnosis) are recommended.
Suggested follow-up evaluations include the following:
Complete physical examination (performed yearly or sooner if clinically indicated):
Blood pressure and other vital signs
Skin examination
No clinical trials have been registered for deficiency of adenosine deaminase 2.
64 publications have been identified in PubMed for deficiency of adenosine deaminase 2. Research spans Case Report / Case Series (45%), Review / Meta-Analysis (22%), and Basic Science / Preclinical (13%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 29 | 45% |
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 12:34 AM UTC
Source: GeneReviews — "Adenosine Deaminase 2 Deficiency"
Intermittent fevers
Hepatosplenomegaly (can be evidence of portal hypertension)
Systemic hypertension
Laboratory findings
Elevated C-reactive protein (CRP) and erythrocyte sedimentation rate during flare episodes
Elevated transaminases
Vasculitis
Clinical findings
Source: GeneReviews — "Adenosine Deaminase 2 Deficiency"
Inherited disorders to consider in the differential diagnosis of DADA2 are included in ; disorders without a known genetic component to consider in the differential diagnosis are discussed following . Table 2. Inherited Disorders with Normal ADA2 Enzyme Activity to Consider in the Differential Diagnosis of Adenosine Deaminase 2 Deficiency (DADA2)
DiffDx Disorder | Gene(s) | MOI | Clinical Features of DiffDx Disorder |
|---|---|---|---|
Overlapping w/DADA2 | Distinguishing from DADA2 Diamond-Blackfan anemia (DBA) | 12 ribosomal protein genes,GATA1,TSR2 | AD |
ADA | AR | Immune deficiency | Immune deficiency is much more severe.; Depletion of T, B, NK cells; Low levels of ADA; Lack cerebrovascular disease cutaneous manifestations GATA2 deficiency (OMIM 614172) |
GATA2 | AD | Immune deficiency, cytopenia, recurrent infections2 | Infections are often invasive. |
Vasculitic complications are rare. Autoimmune lymphoproliferative syndrome (ALPS) | CASP10,FAS,FASLG3 | ADAR | Lymphadenopathy, splenomegaly, immune-mediated cytopenia4 |
Source: GeneReviews — "Adenosine Deaminase 2 Deficiency"
Biomarker and diagnostic research for deficiency of adenosine deaminase 2 has been reported in the published literature.
Blood pressure and other vital signs, as systemic hypertension and/or fever are common.
Skin examination for evidence of livedo reticularis/racemosa, nodules, and Raynaud phenomenon. Severe involvement can include digital infarcts/gangrene or skin ulcerations.
Assessment for lymphadenopathy and hepatosplenomegaly.
Neurologic examination for evidence of prior or recent strokes.
Ophthalmologic examination for vision loss, diplopia, retinal infarcts, optic nerve damage, uveitis, ptosis, strabismus, and nystagmus
Electrocardiogram (ECG) for manifestations of portal hypertension, including prolonged QT interval
• Laboratory assessment
Source: GeneReviews — "Adenosine Deaminase 2 Deficiency"
Avoid the following:
Antiplatelet medications including aspirin
Anticoagulation medications (except in the presence of atrial fibrillation)
Smoking, which may exacerbate peripheral arterial disease
Source: GeneReviews — "Adenosine Deaminase 2 Deficiency"
Search ClinicalTrials.gov in the US and EU Clinical Trials Register in Europe for access to information on clinical studies for a wide range of diseases and conditions. Note: There may not be clinical trials for this disorder.
Source: GeneReviews — "Adenosine Deaminase 2 Deficiency"
View trials for deficiency of adenosine deaminase 2
Neurologic examination for evidence of prior or recent strokes
Ophthalmologic examination for ptosis, abnormal eye movements, retinal infarcts, optic nerve damage
ECG (if abnormal in the past). Note: Arterial hypertension, reported in 20% of patients, can lead to myocardial dysfunction.
Laboratory assessment (performed yearly or sooner if clinically indicated):
CBC and differential
ESR and CRP
Kidney and liver function
Quantitative serum immunoglobulins
Lymphocyte phenotyping for evidence of a B-cell maturation defect
Additionally, follow-up evaluation of abnormal laboratory studies identified at earlier evaluations
Imaging assessment (yearly or if clinically indicated):
Brain MRI if abnormal in the past or new symptoms or manifestations suggest brain involvement
Peripheral MRA if symptoms of peripheral arterial disease and/or neurologic dysfunction
Abdominal ultrasound examination to assess liver, spleen, and kidney size and hepatic blood flow
FibroScan® ultrasound examination (if available) to assess hepatic elasticity for evidence of early portal hypertension
Liver biopsy (if clinically indicated) is the most reliable way to diagnose diffuse hepatic disease (e.g., in the presence of portal hypertension).
Source: GeneReviews — "Adenosine Deaminase 2 Deficiency"
Research summaries
14 |
22% |
Laboratory research | 8 | 13% |
Disease patterns and progression | 5 | 8% |
Testing and diagnosis research | 4 | 6% |
Other research | 3 | 5% |
New treatment approaches | 1 | 2% |
Lim J (2026). [PMID: 41484495](https://pubmed.ncbi.nlm.nih.gov/41484495/). *Curr Allergy Asthma Rep*. [Review / Meta-Analysis]
Muniraju T (2026). [PMID: 42055761](https://pubmed.ncbi.nlm.nih.gov/42055761/). *BMJ Case Rep*. [Case Report / Case Series]
Türkmen Ş (2026). [PMID: 42084883](https://pubmed.ncbi.nlm.nih.gov/42084883/). *Turk Arch Pediatr*. [Epidemiology / Natural History]
Lim TT (2026). [PMID: 42033811](https://pubmed.ncbi.nlm.nih.gov/42033811/). *Acta Neurol Taiwan*. [Case Report / Case Series]
Shaik MR (2026). [PMID: 42083127](https://pubmed.ncbi.nlm.nih.gov/42083127/). *Liver Int*. [Case Report / Case Series]
Ehlers L (2026). [PMID: 41866403](https://pubmed.ncbi.nlm.nih.gov/41866403/). *Cell Death Discov*. [Case Report / Case Series]
Sparchez M (2026). [PMID: 41594165](https://pubmed.ncbi.nlm.nih.gov/41594165/). *Diagnostics (Basel)*. [Case Report / Case Series]
Koga T (2026). [PMID: 41620931](https://pubmed.ncbi.nlm.nih.gov/41620931/). *Expert Rev Clin Immunol*. [Review / Meta-Analysis]
Yue J (2026). [PMID: 41147740](https://pubmed.ncbi.nlm.nih.gov/41147740/). *Arthritis Rheumatol*. [Diagnostic / Biomarker]
Engelstein DK (2026). [PMID: 41539726](https://pubmed.ncbi.nlm.nih.gov/41539726/). *J Rheumatol*. [Epidemiology / Natural History]
AI-curated news mentioning deficiency of adenosine deaminase 2
Updated May 5, 2026
A recent study published in PubMed explores the hepatic manifestations and treatment responses in patients with adenosine deaminase 2 deficiency. This research contributes to understanding the disease's impact on liver function and potential therapeutic approaches.
A recent study published in PubMed explores multisystem vasculopathy associated with adenosine deaminase 2 deficiency. This research contributes to the understanding of the disease's pathophysiology and potential therapeutic targets.