Hereditary angioedema (HAE) is a rare but potentially life-threatening genetic disorder causing recurrent episodes of severe swelling of the skin and mucosa.1 It results from either a deficiency (type 1) or dysfunction (type II) of C1 esterase inhibitor (C1-INH).1,2 Diagnosis traditionally relies on

The current gold standard for diagnosing food allergy (FA) is through oral food challenges (OFCs). To minimize the impact of potential allergic reactions mid-diagnosis, OFCs are performed under the presence of the appropriate equipment, trained personnel and readily available emergency treatment...

STUDY DESIGN Compared to their adult counterparts, children and adolescents with type 2 diabetes mellitus (T2DM) experience an accelerated deterioration in beta-cell function and development of insulin resistance, thereby elevating their risk of early-onset complications. Currently, treatment optio

STUDY DESIGN Despite an increasing incidence of type 2 diabetes mellitus (T2D) among children and adolescents, treatment options for this population remain limited.1 The T2NOW study was a 26-week, double-blinded, phase 3 study that investigated the efficacy and safety of dapagliflozin (DAPA) or sax

A recent randomized clinical trial suggests that undergoing testing for specific nasopharyngeal bacteria in children with acute sinusitis could identify those who will benefit most from antibiotic treatment.1 Consequently, this could in turn substantially reduce antibiotic use among pediatric patien