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Results for “Rare Fetal Genetic Diseases”

7 trials

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Showing 7 of 7 results

Not applicableUnknownNCT04406480
What this trial is testing

Realization of Sequencing of All Known Human Genes in Case of Detection of Cerebral, Renal or Ophthalmological Fetal Malformations During Pregnancy in Order to Make an Etiological Diagnosis and to Precise the Fetal Prognosis

Who this might be right for
Fetal MalformationPregnancy RelatedRare Genetic Disease
University Hospital, Strasbourg, France 90
Not applicableStudy completedNCT06831799
What this trial is testing

ERN-EuroBloodNet Registry on Patients With Rare Red Blood Cell Defects and COVID-19

Who this might be right for
HemoglobinopathiesSickle Cell DiseaseSickle Cell Anemia+21 more
Hospital Universitari Vall d'Hebron Research Institute 684
Not applicableLooking for participantsNCT01793168
What this trial is testing

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

Who this might be right for
Rare DisordersUndiagnosed DisordersDisorders of Unknown Prevalence+340 more
Sanford Health 20,000
Not applicableUnknownNCT00005105
What this trial is testing

Genetic Study of Insulin-Like Growth Factor-I Receptor Mutations in Patients With Intrauterine Growth Retardation

Who this might be right for
Intrauterine Growth Retardation
National Center for Research Resources (NCRR) 75
Testing effectiveness (Phase 2)Study completedNCT00004381
What this trial is testing

Phase II Randomized Study of Tin Mesoporphyrin for Neonatal Hyperbilirubinemia

Who this might be right for
Glucosephosphate Dehydrogenase DeficiencyHyperbilirubinemiaHemolytic Disease of Newborn
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Not applicableUnknownNCT03688594
What this trial is testing

Non Invasive Prenatal Test of Rare Genetic Diseases: Application to Rare Intellectual Disabilities

Who this might be right for
Genetic Disorders in Pregnancy
University Hospital, Strasbourg, France 60
Not applicableLooking for participantsNCT06475651
What this trial is testing

Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With Prenatal Onset

Who this might be right for
Rare Fetal Genetic DiseasesCongenital Malformation
Assistance Publique - Hôpitaux de Paris 63