Epidermolysis Bullosa, Junctional Epidermolysis bullosa, junctional, is a genetic skin disorder causing fragile skin․ Learn […]
Understanding Neuhauser-Eichner-Opitz Syndrome: A Rare Genetic Neurological Disorder
Introduction Neuhauser-Eichner-Opitz Syndrome, also known as recurrent encephalopathy of childhood, is a rare genetic neurological […]
Understanding Epidermolysis Bullosa Simplex with Anodontia and Hair
Disease ー Epidermolysis Bullosa Simplex with Anodontia and Hair Epidermolysis bullosa simplex with anodontia is […]
Understanding Ocular Complications in Nephrotic Syndrome
Introduction Nephrotic syndrome is the most common glomerulopathy among children aged 2-18 years. Potentially blinding […]
Understanding Nephrosclerosis: Causes, Symptoms, and Diagnostic Approaches
Introduction to Nephrosclerosis Nephrosclerosis is a progressive renal impairment caused by chronic‚ poorly controlled hypertension. […]
Managing Epidermolysis Bullosa Pretibial: Symptoms, Treatment, and Diagnosis
Managing Epidermolysis Bullosa Pretibial Epidermolysis Bullosa (EB) is a rare genetic disorder that causes fragile […]
Understanding 3 Beta Hydroxysteroid Dehydrogenase Deficiency: Symptoms, Treatment, Causes, Diagnosis, and Prognosis
Symptoms of 3 Beta Hydroxysteroid Dehydrogenase Deficiency Look out for signs like salt-wasting, dehydration, ambiguous […]
Introduction to Netherton Syndrome Ichthyosis
Netherton Syndrome Ichthyosis is a rare genetic condition impacting the skin, hair, and immune system․ […]
Understanding Nephropathy Familial with Hyperuricemia
Introduction Nephropathy familial with hyperuricemia is a rare inherited kidney disease characterized by early-onset gout, […]
Understanding Epidermolysis Bullosa‚ Generalized Atrophic Benign
Understanding Epidermolysis Bullosa‚ Generalized Atrophic Benign Epidermolysis Bullosa‚ Generalized Atrophic Benign is a rare genetic […]