genetic testing

Leigh syndrome, first described by Denis Leigh in 1951, is a severe progressive neurometabolic disorder characterized by bilateral symmetric necrotic lesions in subcortical regions of the central nervous system. Originally termed subacute necrotizing encephalomyelopathy, this disorder represents a final common phenotype for various genetic defects affecting energy metabolism.

The prostate gland, an integral component of the male reproductive system, can develop malignant tumors that significantly impact urological health. This comprehensive guide examines prostate cancer's anatomical presentation, diagnostic approaches, and current treatment modalities, providing essential information for medical professionals and students in understanding this prevalent male cancer.

The intricate relationship between genetics and eczema has become increasingly clear through advanced medical research and genetic studies. Scientists have discovered that multiple genes work in concert to influence both the development and severity of eczema, making it a complex inherited condition that affects millions worldwide.

Understanding rare genetic conditions is crucial for healthcare providers and families alike. ARTX syndrome, also known as ATRX syndrome or Alpha-Thalassemia X-Linked Intellectual Disability syndrome, is a rare genetic condition that primarily affects males. This comprehensive guide explores the causes, symptoms, diagnosis, and management options for individuals living with ARTX syndrome.