Introduction Stoll–Levy–Francfort Syndrome is a rare condition characterized by limb, ear, and heart anomalies. Learn […]
Understanding Stormorken-Sjaastad-Langslet Syndrome
Introduction Stormorken-Sjaastad-Langslet syndrome is a rare autosomal dominant disease characterized by a complex phenotype․ Also […]
Overview of Stoll–Geraudel–Chauvin Syndrome
A rare genetic syndromic intellectual disability impacting males characterized by short stature, mild to moderate […]
Alopecia⁚ Causes, Treatments, and Prevention Tips
Alopecia can be caused by genetics, hormonal changes, or medical conditions. Causes of Alopecia Alopecia […]
Understanding Neuroacanthocytosis
Neuroacanthocytosis (NA) syndromes are genetically defined diseases characterized by red blood cell changes and basal […]
Overview of Neuraminidase Beta-Galactosidase Deficiency
Galactosialidosis, also known as neuraminidase deficiency with beta-galactosidase deficiency, is a genetic lysosomal storage disease. […]
Overview of Adult-Onset Stills Disease
Overview of Stills Disease Adult-onset Stills disease (AOSD) is a form of Stills disease, a […]
Understanding Neuhauser–Daly–Magnelli Syndrome
Overview of Neuhauser–Daly–Magnelli Syndrome Megacornea Mental Retardation Syndrome, known as Neuhauser Syndrome, is a rare […]
Understanding Stiff Skin Syndrome: Symptoms, Diagnosis, and Treatment
Introduction to Stiff Skin Syndrome Scleroderma, which literally means a pathological hardening of the skin, […]
Understanding Congenital Short Bowel Syndrome: Causes, Symptoms, Diagnosis, Treatment, and Management
Plan⁚ Causes, Symptoms, Diagnosis, Treatment, and Management of Congenital Short Bowel Syndrome Exploring the varied […]