Disease ⏤ Encephalitis Lethargica Encephalitis Lethargica, a rare neurological disorder, is the primary focus of […]
Understanding Emery-Dreifuss Muscular Dystrophy: Symptoms, Diagnosis, and Treatment
Introduction Learn about Emery–Dreifuss muscular dystrophy, an X-linked genetic disease affecting skeletal and cardiac muscle. […]
Understanding Enamel Hypoplasia Cataract Hydrocephaly (EHCH): Diagnosis, Treatment, and Complications
Enamel Hypoplasia Cataract Hydrocephaly Enamel hypoplasia cataract hydrocephaly (EHCH) is a rare congenital syndrome with […]
Understanding Turner Syndrome: Causes, Symptoms, Diagnosis, and Treatment
Introduction Turner syndrome, a genetic disorder that affects only females, occurs when one of the […]
Understanding Femur-Fibula-Ulna (FFU) Syndrome: Characteristics, Diagnosis, and Genetic Testing
Introduction Clinica Imagenologica Dres. Parada, Montevideo, Uruguay. Definition⁚ Unilateral or bilateral short lower extremity due […]
Understanding Ulerythema Ophryogenesis: Symptoms, Diagnosis, and Management
Introduction Ulerythema ophryogenesis is a rare cutaneous atrophic disorder associated with Noonan syndrome, characterized by […]
Managing Chest Tightness in Emphysema Patients
Managing Chest Tightness in Emphysema Patients Emphysema is a disease that affects breathing. Understanding its […]
Understanding Ulna Metaphyseal Dysplasia Syndrome: Symptoms, Diagnosis, and Management
Introduction Disease⁚ Ulna Metaphyseal Dysplasia Syndrome Ulna metaphyseal dysplasia syndrome, also known as Rosenberg-Lohr Syndrome, […]
Understanding Empty Sella Syndrome: Causes, Symptoms, and Management
Disease, Empty Sella Syndrome Empty Sella Syndrome occurs when the pituitary gland shrinks or flattens […]
Understanding Emerinopathy: Genetic Basis, Pathophysiology, and Therapeutic Implications
Disease ⎻ Emerinopathy I. Introduction to Emerinopathy Emerinopathy is a rare genetic disorder characterized by […]