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1. Severe T-cell lymphopenia in a patient with microduplication 22q11.2 identified by newborn screening.

Author

Soomann M, Prader S, Lorenzini T, Soulard C, Sayasith K, Haddad E, and Pachlopnik Schmid J

Subjects
Humans, Infant, Newborn, Chromosome Duplication, Male, Female, Lymphopenia genetics, Lymphopenia diagnosis, Neonatal Screening, Chromosomes, Human, Pair 22 genetics, T-Lymphocytes immunology, DiGeorge Syndrome genetics, DiGeorge Syndrome diagnosis, DiGeorge Syndrome immunology, DiGeorge Syndrome complications
Published
2024
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