Background: Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive genodermatosis characterized by poikiloderma, sparse hair, skeletal anomalies, and an increased risk of malignancies, particularly osteosarcoma and skin cancers. RTS is classified into two types: Type I wit...
Open access
Research Article10.9734/ajpr/2025/v15i6451
Background: Neonatal lupus erythematosus (NLE) is a rare autoimmune condition resulting from the transplacental transfer of maternal autoantibodies, primarily anti-SSA/Ro and anti-SSB/La. The disease can manifest with cutaneous, cardiac, hematologic, and hepatobiliary involvement...
Open access
Research Article10.9734/ajpr/2025/v15i5447
Background: Pemphigus foliaceus (PF) is a rare autoimmune blistering disorder caused by IgG4 autoantibodies targeting desmoglein 1, leading to superficial intraepidermal acantholysis. While typically presenting with widespread lesions, localized forms are exceptionally rare. Obje...
Open access
Research Article10.9734/ajrdes/2025/v8i1125