Medical Genetics
Favism: Clinical Manifestations and Management of Glucose-6-Phosphate Dehydrogenase Deficiency
Favism is a genetic disorder that causes a severe reaction to consuming fava beans (also known as broad beans) and certain medications. This inherited condition occurs due to a deficiency in an enzyme called glucose-6-phosphate dehydrogenase (G6PD), which leads to the breakdown of red blood cells when exposed to specific triggers.
Children diseases
ARTX Syndrome: Understanding a Rare X-Linked Intellectual Disability
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.