Medical Syndrome-I

Iatrogenic Cushing’s Syndrome: An Introduction Iatrogenic Cushing’s Syndrome might sound unfamiliar, but its implications can be significant for those who rely on long-term steroid therapies. As the medical community increasingly recognizes this condition, it’s vital to understand how exogenous glucocorticoids can lead to a range of health issues that go beyond their intended use. While

Idiopathic Hypersomnia Syndrome is more than just an overwhelming need for sleep. It’s a complex neurological disorder that significantly impacts the lives of those affected. While many people may dismiss excessive daytime sleepiness as mere fatigue, individuals with this condition often struggle to navigate daily activities, relationships, and work responsibilities due to their persistent drowsiness.

IRIS Syndrome, or Immune Reconstitution Inflammatory Syndrome, is a complex and often misunderstood condition that emerges when the immune system begins to recover after intensive treatment. For many patients with compromised immunity—especially those with HIV/AIDS—the onset of IRIS can be both surprising and alarming. It represents a paradox where the restoration of immune function triggers

Inclusion-Cell Syndrome, often referred to as I-Cell Disease, is a rare genetic disorder that affects multiple systems in the body. It primarily stems from issues with lysosomal enzyme functioning, which leads to a cascade of health challenges for those affected. While it may not be widely known, understanding this condition is crucial for patients and

Immune Dysregulation Syndrome is an intricate condition that affects the body’s ability to maintain a balanced immune response. This can lead to a range of health issues, from autoimmune diseases to various complications affecting multiple organ systems. Understanding this syndrome is crucial for patients and healthcare providers alike, as it provides insights into diagnosis, management,

ICF Syndrome, short for Immunodeficiency, Centromeric instability, and Facial anomalies, is a rare genetic disorder that presents unique challenges for those affected. Understanding this syndrome is crucial not only for patients but also for families and healthcare providers. In this comprehensive guide, we will explore the underlying genetic basis of ICF Syndrome, its clinical features,