Chromosome 3 Monosomy 3p25 Overview Chromosome 3 Monosomy 3p25 is a rare genetic condition that […]
Understanding Nystagmus: Causes, Symptoms, and Treatment
Introduction Nystagmus is defined by rhythmic, abnormal eye movements with a slow eye movement driving […]
Exploring the Link Between Facial Asymmetry and Temporal Lobe Seizures
Facial Asymmetry and Temporal Lobe Seizures When dealing with the complex interplay of facial asymmetry […]
Understanding Notalgia Paresthetica: Symptoms, Causes, and Treatment Options
Introduction to Notalgia Paresthetica Notalgia paresthetica is a chronic sensory neuropathy mainly affecting the area […]
Understanding Factor II Deficiency: Causes, Symptoms, and Management
Understanding Factor II Deficiency Factor II deficiency is a genetic disorder that affects blood clotting, […]
Understanding Faciocardiorenal Syndrome: Genetics, Symptoms, and Treatment
Faciocardiorenal Syndrome Introduction FacioCardioRenal Syndrome‚ also known as FCAS‚ is a rare genetic disorder that […]
Understanding the Unusual Facial Features in Arthrogryposis
Disease ⎼ Facies unusual arthrogryposis advanced skeletal malformations Introduction Welcome to this comprehensive article on […]
Faciooculoacousticorenal Syndrome: Understanding a Rare Genetic Disorder
Faciooculoacousticorenal Syndrome is a rare genetic disorder affecting multiple organs. This article delves into its […]
Understanding Syndactyly: Types, Prevalence, and Genetic Factors
Introduction to Syndactyly Syndactyly is one of the most common congenital anomalies, presenting with the […]
Introduction to Syncopal Paroxysmal Tachycardia
Disease⁚ Syncopal paroxysmal tachycardia Syncopal paroxysmal tachycardia, characterized by sudden onset and termination of supraventricular […]