Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome (VAIHS)

Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome(来自ICD-11)

别称:

Adenosine Deaminase 2 Deficiency

Ada2 Deficiency

Dada2

Pan

Polyarteritis Nodosa, Childhood-Onset

Deficiency of Adenosine Deaminase 2

Polyarteritis Nodosa

Deficiency of Ada2

Sneddon Syndrome

Vaihs

Childhood-Onset Polyarteritis Nodosa

Vasculitis Due to Ada2 Deficiency

Periarteritis Nodosa

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome, also known as adenosine deaminase 2 deficiency, is related to sneddon syndrome and cutaneous polyarteritis nodosa, and has symptoms including headache, hemiplegia and seizures. An important gene associated with Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome is ADA2 (Adenosine Deaminase 2). The drugs Azathioprine and Prednisolone have been mentioned in the context of this disorder. Affiliated tissues include skin and liver, and related phenotypes are anemia and aphasia

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