Bell’s Palsy and Ramsay Hunt Syndrome

Abstract Bell’s Palsy and Ramsay Hunt Syndrome (RHS) are two distinct causes of peripheral facial nerve palsy. While both affect the facial nerve and result in facial weakness, their etiology, clinical presentation, and management differ significantly. This article provides a…

Infant Botulism Associated with Honey Ingestion

Introduction Infant botulism is a rare but potentially life-threatening neuromuscular disorder that occurs in infants, typically under one year of age. It is caused by neurotoxins produced by Clostridium botulinum, an anaerobic, spore-forming gram-positive bacillus. Unlike foodborne botulism in adults,…

Candidial Intertrigo

Abstract Candidial intertrigo is a superficial fungal infection that affects intertriginous areas—regions where skin folds rub together and retain moisture. It is commonly caused by Candida albicans and presents as erythematous, macerated plaques with satellite pustules. The condition is particularly…

Hypokalemic Paralysis Due to Use of Furosemide and Salbutamol

Abstract Hypokalemic paralysis is a rare but potentially life-threatening condition characterized by acute onset of muscle weakness due to significantly low serum potassium levels. While it can arise from various etiologies, certain medications such as loop diuretics and beta-agonists can…

Oral Contraceptive Pill Failure Due to Anti-Koch’s Therapy

Introduction: Oral contraceptive pills (OCPs) are a widely used and reliable method of contraception. However, their effectiveness can be compromised by drug interactions. A notable example is the interaction between OCPs and anti-tubercular therapy, specifically rifampicin, a cornerstone drug in…

SGLT2 Inhibitors in Heart Failure

Introduction Heart failure occurs when the heart cannot pump blood efficiently to meet the body’s needs. It leads to symptoms like fatigue, breathlessness, swelling, and frequent hospitalizations. In recent years, a group of medications called SGLT2 inhibitors—originally used for diabetes—have…

Bardet-Biedl Syndrome

Introduction Bardet-Biedl Syndrome (BBS) is a rare, genetically heterogeneous disorder characterized by a constellation of features affecting multiple organ systems. It is primarily inherited in an autosomal recessive pattern and classified as a ciliopathy, due to defective function of primary…

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