PedAM
Pediatric Disease Annotations & Medicines
| Disease | lymphopenia |
| Phenotype | C0085110|severe combined immunodeficiency |
| Sentences | 3 |
| PubMedID- 25170474 | Since its introduction as a public health programme in the united states in the early 1960s, newborn blood screening (nbs) has evolved from the detection of phenylalanine levels on filter paper to the application of dna-based technologies to identify t-cell lymphopenia in infants with severe combined immunodeficiency. |
| PubMedID- 20864885 | Recent findings: as a concept, newborn blood screening (nbs) has evolved from the detection of elevated levels of phenylalanine on filter paper to the application of dna-based technologies to identify t-cell lymphopenia in infants with severe combined immunodeficiency (scid). |
| PubMedID- 24506932 | Results: despite the severe peripheral b-cell lymphopenia, patients with ada-deficient severe combined immunodeficiency showed a partial block in central bm development. |
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