Introduction Myorhythmia‚ a hyperkinetic involuntary movement disorder‚ is characterized by slow rhythmic movements affecting cranial […]
Understanding 21-Hydroxylase Deficiency: Causes, Symptoms, Diagnosis, Treatment, and Long-term Management
Causes of 21-Hydroxylase Deficiency Genetic factors and inherited traits contributing to 21-Hydroxylase Deficiency 21-Hydroxylase Deficiency […]
Understanding Myopathy: Types, Symptoms, and Causes
Understanding Myopathy Myopathy refers to a range of muscle disorders affecting voluntary movement. These conditions […]
Genetic Causes of Chromosome 20 Duplication
The genetic causes of Chromosome 20 duplication involve abnormalities in the DNA structure of the […]
Understanding Myositis Ossificans Progressiva: A Rare Heritable Disorder
Introduction Myositis Ossificans Progressiva, formerly known as Fibrodysplasia Ossificans Progressiva, is an extremely rare heritable […]
Understanding 22q11.2 Deletion Syndrome
Understanding 22q11.2 Deletion Syndrome 22q11.2 Deletion Syndrome is a genetic disorder with various manifestations. It […]
Causes, Symptoms, Diagnosis, Treatment, and Complications of Congenital Mitral Stenosis
Causes of Congenital Mitral Stenosis Understanding the causes‚ such as genetic factors and developmental abnormalities‚ […]
Understanding Cardioauditory Syndrome: Symptoms, Causes, Diagnosis, and Treatment
Symptoms of Cardioauditory Syndrome Common symptoms of Cardioauditory Syndrome include dizziness‚ fainting‚ hearing loss‚ and […]
Understanding Spirurida Infections: A Comprehensive Overview
Introduction to Spirurida Infections Spirurida infections‚ caused by parasitic nematodes‚ pose significant medical challenges. Onchocerca […]
Understanding Splenogonadal Fusion Limb Defects Micrognatia Syndrome
Introduction to Splenogonadal Fusion Limb Defects Micrognatia Splenogonadal fusion-limb defects-micrognatia syndrome is a rare dysostosis […]