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Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders
This study is ongoing, but not recruiting participants.
Study NCT00004341   Information provided by Office of Rare Diseases (ORD)
First Received: October 18, 1999   Last Updated: June 23, 2005   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
X-Linked Agammaglobulinemia
X-Linked Hyper IgM Syndrome
Wiskott-Aldrich Syndrome
Additional conditions recognized in this trial
Adhesions
Agammaglobulinemia
Hyper-IgM Immunodeficiency Syndrome
Hyper-IgM Immunodeficiency Syndrome, Type 1
Immunologic Deficiency Syndromes
Leukocyte-Adhesion Deficiency Syndrome
Syndrome
More general conditions related to this trial
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Blood Platelet Disorders
Blood Protein Disorders
Disease
Dysgammaglobulinemia
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Hematologic Diseases
Hemorrhagic Disorders
Immune System Diseases
Lymphatic Diseases
Lymphoproliferative Disorders
Pathologic Processes
Purpura, Thrombocytopenic
Thrombocytopenia
Sponsors listed in this trial
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
University of Washington


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