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T-Cell Lymphopenia Detected by Newborn Screening in Two Siblings with an Xq13.1 Duplication
Newborn screening for severe combined immunodeficiency has proven successful in identifying infants with T-cell deficiencies before they become severely ill. Additionally, the newborn screen can detect subtle early phenotypes that may become severe later in life. We present the case of siblings with...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513981/ https://www.ncbi.nlm.nih.gov/pubmed/28770187 http://dx.doi.org/10.3389/fped.2017.00156 |