Background: Multiple acyl-CoA dehydrogenase deficiency (MADD), also known as glutaric acidaemia type II (GA II), is a rare inherited autosomal recessive disorder involving the metabolic pathways of fatty acid and amino acid oxidation. Catastrophic metabolic crises are observed in...
Open access
Research Article10.9734/ajrimps/2026/v15i3412
Background: The BAV–VSD–PDA complex, presenting with severe symptomatic AR and severe LVD in a paediatric patient younger than 10 years, is a very uncommon complex congenital structural heart defect. Aim: This report aims to highlight surgical management strategies and a successf...
Open access
Research Article10.9734/ajpr/2026/v16i9567
Background: Acute suppurative parotitis is uncommon in infants and is rarely observed beyond the neonatal period. When bilateral, its clinical presentation may resemble viral parotitis, cervical lymphadenitis, or deep-neck-space infection. Early high-resolution ultrasonography ma...
Open access
Research Article10.9734/ijmpcr/2026/v19i3510
Background: Tubercular meningitis (TBM) is the most severe form of central nervous system tuberculosis, and its course is frequently complicated by vasculitis, tuberculomas, and ischaemic infarcts. When acute vasculitic cortical-subcortical infarcts occur alongside active cavitar...
Open access
Research Article10.9734/ijmpcr/2026/v19i3506
Background: Postpartum cardiomyopathy (PPCM) presents in late pregnancy or the postpartum period and is a rare, sometimes fatal cause of idiopathic heart failure. Septic cardiomyopathy is a reversible impairment of myocardial function occurring with severe sepsis. The coexistence...
Open access
Research Article10.9734/ijmpcr/2026/v19i3521