Most recent by Nicholas L. Hartog, MD, FAAAAI, FACAAI
Disparities persist in testing for inborn errors of immunity despite sponsored program
Significant racial disparities persisted in genetic testing for inborn errors of immunity despite the removal of financial barriers, according to a study published in The Journal of Allergy and Clinical Immunology: In Practice.
Genetic testing is key to diagnosing primary immunodeficiencies
There are more than 450 monogenetic immune deficiencies. While many of these rare conditions have similar hallmarks, it is crucial for clinicians to differentiate between them.
Analytical pipeline conducts population-wide immunodeficiency screenings
A two-step analytical pipeline facilitated the identification of individuals with primary immunodeficiency and accurately quantified their clinical risk, according to a study published in The Journal of Allergy & Clinical Immunology.
Q&A: Expanded rollout of adenosine deaminase deficiency newborn screenings recommended
Tandem mass spectroscopy screenings for newborns can identify partial or delayed adenosine deaminase deficiencies, which can have potentially fatal complications, according to a review published in Annals of Allergy, Asthma & Immunology.