Introduction Triopia is a rare condition that affects development in the womb. Babies born with […]
Understanding Dystonia with Progressive Diurnal Variation
Disease ⎼ Dystonia with Progressive Diurnal Variation Understanding Dystonia Dystonia is a neurological disorder characterized […]
Understanding Dystrophia Myotonica: Genetic Basis, Clinical Manifestations, and Management
Understanding Dystrophia Myotonica Dystrophia Myotonica (DM1) is a genetic disorder characterized by muscle weakness, myotonia, […]
Dysplasia: Understanding Abnormal Cellular Growth
Disease ⸺ Dysplasia Dysplasia refers to the abnormal development or growth of cells within a […]
Understanding Dysprothrombinemia: Genetic Basis, Symptoms, and Treatment Options
Disease ⸺ Dysprothrombinemia Dysprothrombinemia is a rare disorder characterized by a genetic deficiency in the […]
Health Topics
This article will cover a range of essential health topics including Understanding Basal Cell Carcinoma‚ […]
Overview of Spastic Diplegia Infantile Type
Spastic diplegia is a form of cerebral palsy characterized by muscle tightness, especially in the […]
Understanding Monosomy 2q37: Symptoms, Genetic Counseling, and Treatment Options
Common Symptoms of Monosomy 2q37 Include⁚ Global developmental delays Low muscle tone Distinct facial features […]
Understanding Spastic Ataxia Charlevoix-Saguenay Type
Overview of Spastic Ataxia Charlevoix–Saguenay Type Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a […]
Understanding Merosin-Positive Congenital Muscular Dystrophy
Introduction to Merosin-positive Congenital Muscular Dystrophy Merosin-positive congenital muscular dystrophy presents a range of clinical […]