Immunologic Evaluation in Patients With DiGeorge Syndrome or Velocardiofacial Syndrome
NCT00005102 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 11
Last updated 2005-06-24
Summary
OBJECTIVES:
I. Determine the pattern of immunologic reconstitution in patients with T-cell compromise due to DiGeorge syndrome or velocardiofacial syndrome.
II. Determine any correlation between immunologic function in these patients and chromosome 22 deletion breakpoints.
III. Determine presence of sustained immunologic compromise in older patients.
Conditions
- DiGeorge Syndrome
- Shprintzen Syndrome
- Chromosome Abnormalities
- Abnormalities, Multiple
- Conotruncal Cardiac Defects
Sponsors & Collaborators
-
Children's Hospital of Philadelphia
collaborator OTHER -
National Center for Research Resources (NCRR)
lead NIH
Principal Investigators
-
Kathleen E. Sullivan · Children's Hospital of Philadelphia
Eligibility
- Min Age
- 0 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1995-01-31
Countries
- United States
Study Locations
More Related Trials
-
Dyskinesia, Heterotaxy and Congenital Heart Disease
NCT00608556 ·Status: COMPLETED
-
Congenital Heart Disease GEnetic NEtwork Study (CHD GENES)
NCT01196182 ·Status: ACTIVE_NOT_RECRUITING
-
Pediatric Cardiomyopathy Mutation Analysis
NCT02432092 ·Status: RECRUITING
-
Cardiac Allograft Remodeling and Effects of Sirolimus
NCT01889992 ·Status: TERMINATED ·Phase: PHASE1
-
Rhythm Disturbances After Ventricular Septal Defects
NCT00208624 ·Status: TERMINATED
-
Genetics of Congenital Heart Disease
NCT01192048 ·Status: RECRUITING
-
Prevalence and Clinical Spectrum of the 22q11 Deletion
NCT00267397 ·Status: TERMINATED
-
Pathophysiology of Dilated Cardiomyopathy
NCT02001961 ·Status: WITHDRAWN
-
Cardiopulmonary Function in Adults Born With a Ventricular Septal Defect
NCT03684161 ·Status: COMPLETED
-
Molecular Basis of Congenital Heart Defects
NCT00579358 ·Status: WITHDRAWN
-
Whole Exome Sequencing and Whole Genome Sequencing for Nonimmune Fetal/Neonatal Hydrops
NCT03911531 ·Status: RECRUITING
-
Heart Failure in Adult Patients With a History of Congenital Heart Disease
NCT00208754 ·Status: TERMINATED
-
Thoracoscopic Vascular Rings Chart Review
NCT00229853 ·Status: TERMINATED
-
Biomarker Study for Heart Failure in Children With Single Ventricle Physiology
NCT00571233 ·Status: COMPLETED
-
Molecular and Cellular Characterization of Cardiac Tissue in Postnatal Development
NCT00243776 ·Status: RECRUITING
-
Molecular Genetics of Heterotaxy and Related Congenital Heart Defects
NCT02432079 ·Status: RECRUITING
-
Examining Developmental Changes in Heart Contractions of Children With Congenital Heart Defects
NCT00860327 ·Status: TERMINATED
-
Constrictive Pericarditis in the Adult Congenital Cardiac Population
NCT00268086 ·Status: TERMINATED
-
Prospective Characterization of the Heart, Aorta and Blood Pressure in Turner Syndrome. Association With Aortic Dissection.
NCT01678274 ·Status: UNKNOWN
-
Outcomes of Children With Congenital Single Ventricle Heart
NCT00266968 ·Status: COMPLETED
-
Surgical Outcomes in Pediatric Patients With Coarctation and VSD
NCT00327795 ·Status: TERMINATED
-
Pulmonary Resistance in Fontan Who Have Undergone Heart Transplantation
NCT00268047 ·Status: TERMINATED
-
Genotype-Phenotype Associations in Pediatric Cardiomyopathy (PCM GENES)
NCT01873963 ·Status: COMPLETED
-
Thoracic Aortic Dilatation Syndromes
NCT02111668 ·Status: COMPLETED
-
Retrospective Evaluation of Carvedilol Versus Captopril in CHF Patients
NCT00249067 ·Status: TERMINATED