Introduction Neurosyphilis is a condition that challenges physicians due to its protean symptoms affecting the […]
Understanding Congenital Spherocytic Anemia: Causes, Symptoms, Diagnosis, and Treatment
Causes of Congenital Spherocytic Anemia Understanding the underlying genetic mutations and hereditary factors is crucial […]
Understanding Monosomy 3p Chromosome 3 Deletion Syndrome and Its Management
Understanding Monosomy 3p Chromosome 3 Deletion Syndrome is crucial for proper diagnosis and management. Overview […]
Understanding Superior Oblique Myokymia: Symptoms, Diagnosis, and Treatment
Introduction Superior oblique myokymia (SOM) is defined as monocular, high-frequency, low-amplitude, torsional, and involuntary contractions […]
Understanding Nevi Flammei: Genetic Background, Inheritance Patterns, and Clinical Descriptions
Introduction Nevi flammei, also known as familial multiple port-wine stains, is a rare genetic capillary […]
Nevus of Ota and Retinitis Pigmentosa: A Rare Association
Nevus of Ota Retinitis Pigmentosa This report describes an association of primary retinitis pigmentosa with […]
Understanding Hereditary Sensory Neuropathy Type II (HSAN II)
Introduction to Hereditary Sensory Neuropathy Type II (HSAN II) Hereditary Sensory and Autonomic Neuropathy (HSAN) […]
Understanding Niemann-Pick C2 Disease: Causes, Symptoms, and Treatment Options
Article Plan⁚ Disease ⎯ Niemann-Pick C2 Disease Overview of Niemann-Pick C2 Disease Niemann-Pick disease type […]
Understanding Sutton Disease: Causes, Diagnosis, Treatment, and Prognosis
Overview of Sutton Disease The prognosis of Sutton Disease includes the duration, complications, recovery period, […]
Understanding Neuropathy, Hereditary Motor and Sensory, LOM Type: A Comprehensive Overview
Introduction Neuropathy, hereditary motor and sensory, LOM type, is a rare and severe form of […]