Immunophenotypic and Molecular Diagnostic Features of Severe Combined Immunodeficiency, Wiskott–Aldrich Syndrome, DOCK8 Deficiency, Activated PI3Kδ Syndrome, and Gray Platelet Syndrome: A Critical Narrative Review
Subham Ganguly, Rojina Khatun & Malavika Bhattacharya · Journal of Advances in Medicine and Medical Research · 2026
Severe combined immunodeficiency, Wiskott–Aldrich syndrome, dedicator of cytokinesis 8 (DOCK8) deficiency, activated phosphoinositide 3-kinase delta syndrome, and gray platelet syndrome are rare monogenic disorders in which diagnosis depends on the combined interpretation of mult...
Open access
Research Article
10.9734/jammr/2026/v38i86178