Researchers are trying to identify versions of genes as well as factors in subjects blood associated with certain types of congenital malformations(CMs). This study will help the researchers to better understand family traits that contribute to CMs.
Study Type
OBSERVATIONAL
Enrollment
132
Mayo Clinic
Rochester, Minnesota, United States
Genetic variants
Identification of genetic variants which may be associated with VACTERL association or other congenital malformations.
Time frame: 2 years
Targeted metabolomics
Identification of changes in metabolic pathways which may provide functional insight into the presence of genetic variants in patients with VACTERL association
Time frame: 2 years
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