Introduction Sotos syndrome, also known as cerebral gigantism, is a rare genetic disorder characterized by […]
Understanding Limb-Girdle Muscular Dystrophy Type 2A
Disease Overview Limb-girdle muscular dystrophy type 2A (LGMD2A) is an autosomal recessive disorder characterized by […]
Understanding Muscular Dystrophy Hutterite Type: Clinical Features, Genetic Basis, and Implications
Introduction A slowly progressive type of muscular dystrophy affecting known members of several Southern Manitoba […]
Understanding Allergic Encephalomyelitis: Causes, Symptoms, and Treatment Options
Introduction to Allergic Encephalomyelitis Definition of Allergic Encephalomyelitis Allergic Encephalomyelitis is an inflammatory condition affecting […]
Understanding Sorsby Fundus Dystrophy: Symptoms, Genetic Inheritance, and Diagnosis
Overview of Sorsby Fundus Dystrophy Sorsby Fundus Dystrophy (SFD) is a rare genetic disorder characterized […]
Understanding Spasmodic Torticollis
Introduction to Spasmodic Torticollis Description and Characteristics of the Disease⁚ Spasmodic torticollis, also known as […]
Understanding Muscular Fibrosis Multifocal Obstructed Vessels
Introduction to Muscular Fibrosis Multifocal Obstructed Vessels Exploring the topic of Muscular Fibrosis Multifocal Obstructed […]
Understanding Merosin-Negative Congenital Muscular Dystrophy
Introduction Congenital muscular dystrophy is a group of early-onset muscle weakness disorders․ Learn about merosin-negative […]
Understanding Craniofacial-Deafness-Hand Syndrome
Introduction Craniofacial-deafness-hand syndrome, also known as Sommer-Young-Wee-Frye syndrome, is a rare autosomal dominant disorder characterized […]