Abstract
CHARGE syndrome is an autosomal dominant condition caused by mutations in chromodomain helicase DNA-binding 7. We report a patient with molecularly confirmed CHARGE syndrome, which included a congenital T cell deficiency, who was treated with peripheral blood mononuclear cell transplantation.
Original language | English (US) |
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Pages (from-to) | 140-142 |
Number of pages | 3 |
Journal | Journal of Pediatrics |
Volume | 154 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2009 |
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health