Introduction: Guillain–Barré syndrome (GBS) is an uncommon, acute autoimmune condition affecting the peripheral nervous system, marked by rapidly progressive, symmetrical muscle weakness and loss of deep tendon reflexes. It frequently occurs following an antecedent infectious epi...
Open access
Research Article10.9734/ijmpcr/2026/v19i2483
Background: Budd-Chiari syndrome is an uncommon condition characterized by thrombotic or non-thrombotic obstruction of hepatic venous outflow. It commonly presents with hepatomegaly, ascites, and abdominal pain. Its incidence is estimated at 1 in 100,000 to 1 in 2.5 million annua...
Open access
Research Article10.9734/ijmpcr/2026/v19i2482
Introduction: Phenytoin is a widely used antiepileptic drug with a narrow therapeutic index and dose-dependent non-linear pharmacokinetics. Even minor changes in metabolism or protein binding may precipitate toxicity and neurological manifestations may mimic cerebellar or cerebro...
Open access
Research Article10.9734/ijmpcr/2026/v19i1480
Introduction: Turner syndrome is a chromosomal disorder caused by partial or complete absence of one X chromosome and is commonly associated with short stature, gonadal dysgenesis, and endocrine abnormalities. Primary amenorrhea is a frequent presenting feature in adolescent fema...
Open access
Research Article10.9734/ijmpcr/2026/v19i1477
Background: First identified by Sharp et al. in 1972, Mixed Connective Tissue Disease (MCTD) is an autoimmune overlap syndrome that is typified by anti-U1RNP antibody positivity and symptoms of polymyositis, systemic lupus erythematosus, and systemic sclerosis. Case Presentation:...
Open access
Research Article10.9734/ijmpcr/2025/v18i4462
Introduction: Aplastic anemia is a rare but serious hematological disorder characterized by bone marrow failure leading to pancytopenia. The condition often presents with nonspecific symptoms, resulting in delayed diagnosis and an increased risk of life-threatening complications....
Open access
Research Article10.9734/ijmpcr/2026/v19i1475