Disease ー Hereditary Hearing Loss Hereditary hearing loss is a genetic condition that can be […]
Understanding Hereditary Non-Spherocytic Hemolytic Anemia: Causes, Symptoms, and Diagnosis
Disease ⎯ Hereditary Non-Spherocytic Hemolytic Anemia Overview of Hereditary Non-Spherocytic Hemolytic Anemia Hereditary non-spherocytic hemolytic […]
Understanding Hereditary Fructose Intolerance (HFI): Causes, Symptoms, and Treatment
Hereditary Fructose Intolerance (HFI) Hereditary fructose intolerance (HFI) is a genetic disorder caused by a […]
Understanding Peripheral Vascular Disease: Causes, Symptoms, and Diagnosis
Article Plan⁚ Disease, Peripheral Blood Vessel Disorder Understanding Peripheral Vascular Disease (PVD) Peripheral vascular disease […]
Understanding VACTERL Association: Symptoms, Diagnosis, and Management
Introduction to VACTERL Association VACTERL association is a condition with multisystem congenital malformations, involving vertebral […]
Understanding Velocardiofacial Syndrome: Symptoms, Prevalence, and Management
Overview of Velocardiofacial Syndrome Velocardiofacial syndrome (VCFS), also known as DiGeorge syndrome or 22q11.2 deletion […]
Understanding Corpus Callosum Dysgenesis: Causes, Symptoms, Diagnosis, Treatment, Prognosis, and Research Advances
Causes of Corpus Callosum Dysgenesis Corpus Callosum Dysgenesis can be caused by genetic mutations, chromosomal […]
Understanding Corpus Callosum Agenesis: Symptoms, Interventions, and Genetic Factors
Look out for intellectual disabilities, seizures, delays in motor skills development, and vision problems. Common […]
Overview of Peripheral T-cell Lymphoma: Symptoms, Diagnosis, Treatment, and Prognosis
Introduction This section provides an overview of Peripheral T-cell Lymphoma, a rare type of non-Hodgkin […]
Understanding Monosomy 8q: Symptoms, Causes, Treatment, and Diagnosis
Symptoms of Monosomy 8q Individuals may experience physical symptoms such as facial abnormalities and skeletal […]