Chromosome 1q23.3q31.1 deletion associated with decreased newborn screening of T cell receptor rearrangement circles (TRECs)

MeSH terms

• Abnormalities, Multiple / diagnosis
• Abnormalities, Multiple / genetics
• Abnormalities, Multiple / immunology*
• Abnormalities, Multiple / pathology
• Chromosome Deletion*
• Chromosomes, Human, Pair 1 / chemistry*
• Female
• Humans
• Infant, Newborn
• Intellectual Disability / diagnosis
• Intellectual Disability / genetics
• Intellectual Disability / immunology*
• Intellectual Disability / pathology
• Lymphopenia / diagnosis
• Lymphopenia / genetics
• Lymphopenia / immunology*
• Lymphopenia / pathology
• Neonatal Screening
• Receptors, Antigen, T-Cell / genetics
• Receptors, Antigen, T-Cell / immunology
• Severe Combined Immunodeficiency / diagnosis
• Severe Combined Immunodeficiency / genetics
• Severe Combined Immunodeficiency / immunology*
• Severe Combined Immunodeficiency / pathology
• T-Lymphocytes / immunology
• T-Lymphocytes / pathology