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
Imperforate hymen is a rare congenital obstructive anomaly of the female genital tract that is usually recognised after menarche, when retained menstrual blood causes haematocolpos and haematometra. Patients commonly present with cyclical lower abdominal pain, primary amenorrhoea...
Open access
Research Article10.9734/ijmpcr/2026/v19i3507
Background: Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are uncommon, life-threatening acute mucocutaneous drug reactions characterised by keratinocyte apoptosis and epidermal separation occurring at the drug-host cell interface. SJS involves less than 10%...
Open access
Research Article10.9734/ijmpcr/2026/v19i3503
Background: Hypokalemic periodic paralysis (HPP) is a skeletal muscle channelopathy characterised by acute episodes of muscle weakness or paralysis associated with severe hypokalaemia. Primary HPP results from inherited ion-channel mutations, whereas secondary HPP is caused by tr...
Open access
Research Article10.9734/ijmpcr/2026/v19i3520