Next Generation Sequencing | Deletion / Duplication | NGS & Del Dup Comprehensive |
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Price: $1100
|
Price: $750
|
Price: $1750
|
CPT: 81406
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CPT: 81405
|
CPT: 81406
81405
|
Glucose/galactose malabsorption is a rare autosomal recessive disorder caused by a defect in glucose and galactose transport across the intestinal brush border. Patients with GGM present with neonatal onset of severe watery diarrhea and dehydration while taking glucose-containing or galactose-containing diets. The condition is life-threatening if not diagnosed and treated. Mutations in the Na+/glucose cotransporter gene SLC5A1 have been determined to cause the disease.
Type E
4 weeks or less