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Results for “Sneddon Syndrome”

4 trials

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Showing 4 of 4 results

Not applicableLooking for participantsNCT06092346
What this trial is testing

A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders

Who this might be right for
AMPD3, OMIM*102772, AMP Deaminase DeficiencyAK1, OMIM *103000, Adenylate Kinase DeficiencyAMPD1, OMIM *102770, Myopathy Due to Myoadenylate Deaminase Deficiency+25 more
National Human Genome Research Institute (NHGRI) 999
Not applicableLooking for participantsNCT06935578
What this trial is testing

RAre, But Not aLone: a Large Italian Network to Empower the Impervious diaGNostic Pathway of Rare cerEbrovascular Diseases (ALIGNED)

Who this might be right for
CADASILCADASIL (Diagnosis)Moya Moya Disease+5 more
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta 500
Not applicableUnknownNCT01952275
What this trial is testing

Observational Study of the Genetic Architecture of Neutrophil-Mediated Inflammatory Skin Diseases

Who this might be right for
Other Specified Inflammatory Disorders of Skin or Subcutaneous TissuePyoderma GangrenosumErosive Pustular Dermatosis of the Scalp+25 more
University of Zurich 600
Not applicableStudy completedNCT06850519
What this trial is testing

Genetic Risk Factors of the Sneddon Syndrome

Who this might be right for
Sneddon Syndrome
Karl Landsteiner University of Health Sciences 40