Overview of Norman-Roberts Lissencephaly Syndrome Norman-Roberts Lissencephaly Syndrome, also known as microlissencephaly type A, is […]
Understanding Nova Syndrome: Genetic and Clinical Implications
Introduction Nova syndrome, also known as Port-Wine Nevi-Mega Cisterna Magna-Hydrocephalus Syndrome, is a rare familial […]
Understanding Norum Disease: Causes, Symptoms, and Management
Introduction Norum disease, a rare lipoprotein metabolism disorder, stems from mutations in the LCAT gene […]
Understanding Bladder Exstrophy Disease
Understanding Bladder Exstrophy Disease This article aims to provide a comprehensive overview of bladder exstrophy, […]
Comprehensive Guide to Facial Cleft: Diagnosis, Treatment, and Care
Disease ⎻ Facial Cleft Facial cleft is a congenital birth defect involving cleft lip and […]
Understanding a Rare Medical Condition: Eye Defects Arachnodactyly Cardiopathy
Disease ─ Eye Defects Arachnodactyly Cardiopathy I․ Overview of the Medical Condition The medical condition […]
Understanding Monosomy 3p2: Chromosome 3 Deletion Syndrome
Monosomy 3p2, also known as Chromosome 3 Deletion Syndrome, is a rare genetic disorder caused […]
Understanding Fabry’s Disease: Genetic Basis, Symptoms, and Management
Fabry’s Disease Understanding Fabry’s Disease involves exploring its genetic basis, lysosomal enzyme deficiency, impact of […]
Understanding Nonverbal Learning Disorder
Introduction to Nonverbal Learning Disorder Nonverbal learning disabilities (NLD) impact the ability to learn from […]
Understanding Nose Polyposis‚ Familial: Hereditary Factors and Genetic Links
Introduction to Nose Polyposis‚ Familial Nasal polyposis‚ familial (also known as nose polyposis‚ familial) is […]