Small and large intestinal diseases concerning for enteropathy or inflammatory bowel disease sometimes can have atypical clinical/histologic presentation and may not respond to conventional treatment. In these instances, the disease may be secondary to inherited primary immune dysfunction or genetic alterations leading to a defect in transport, metabolism, polarity, and function of the mucosal epithelial and endocrine cells. The panel tests for a heterogeneous group of genes related to atypical enteropathy/inflammatory bowel disease such as XIAP deficiency, IPEX syndrome, and ICOS deficiency, among others. This panel includes sequence and deletion/duplication analysis of all the listed genes.
TAT
6 weeks
CPT Code
81443
Test Code
1135
Test Methods
Sequencing
Deletion/Duplication analysis
Specimen Types Accepted
Blood
Saliva
Buccal
Cultured Cells
Extracted DNA
Documents
Genes