Overview of Tetraamelia Ectodermal Dysplasia Tetraamelia Ectodermal Dysplasia is a rare genetic condition affecting skin, […]
Understanding Testotoxicosis: Causes, Symptoms, Diagnosis, and Treatment
Introduction Testotoxicosis (also known as familial male-limited precocious puberty) is a rare condition in boys […]
Understanding Temtamy–Shalash Syndrome: Causes, Symptoms, and Management
Introduction to Temtamy–Shalash Syndrome Temtamy–Shalash Syndrome‚ also known as Craniofacial dysmorphism-coloboma-corpus callosum agenesis syndrome‚ is […]
Understanding Bangstad Syndrome
Understanding Bangstad Syndrome Causes of Bangstad Syndrome Symptoms of Bangstad Syndrome Treatment Options for Bangstad […]
Understanding Telfer-Sugar-Jaeger Syndrome
Overview of Telfer-Sugar-Jaeger Syndrome Piebald trait-neurologic defects syndrome is a rare genetic disorder characterized by […]
Understanding Alternating Hemiplegia: Genetic Factors, Neurological Abnormalities, and Treatment Approaches
Genetic Factors Neurological Abnormalities Triggers and Precipitating Factors Genetic Factors Genetic factors play a significant […]
Banki Syndrome⁚ A Comprehensive Overview
Understanding Banki Syndrome Banki Syndrome is a complex condition with causes that may involve genetic […]
Understanding Tethered Spinal Cord Disease: Causes, Symptoms, and Treatment Options
Introduction The tethered spinal cord disease is a neurologic disorder caused by tissue attachments that […]
Understanding Pontocerebellar Hypoplasia: Clinical Features, Genetic Causes, and Neuropathological Findings
Pontocerebellar hypoplasia (PCH) is a rare group of neurodegenerative disorders characterized by severe hypoplasia or […]
Understanding Daentl Towsend Siegel Syndrome: Characteristics, Speech Impairment, Seizures, and Treatment Options
Daentl Towsend Siegel Syndrome Introduction Daentl Towsend Siegel Syndrome, also known as 17q21․31 microdeletion syndrome, […]