Accutane Embryopathy Accutane embryopathy is a rare disorder and it is also called as Fetal Retinoid Syndrome. Accutane Embryopathy is a characteristic Read More
Accessory Atrioventricular Pathways By definition, accessory atrioventricular pathways are aberrant muscle bundles that connect the atrium to a ventricle outside of the Read More
Agammaglobulinemia Agammaglobulinemia, or hypogammaglobulinemia, is the most common of the primary immunodeficiencies, accounting for approximately 50% of cases. Three major types can Read More
Congenital Afibrinogenemia Congenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to Read More
Alpha High-Density Lipoprotein Deficiency(Tangier Disease) Tangier disease (also known as Familial alpha-lipoprotein deficiency) or hypoalphalipoproteinemia is a rare inherited disorder characterized by Read More
Alpers Disease Alpers disease is a progressive, neurodevelopmental, mitochondrial DNA depletion syndrome characterized by three co-occurring clinical symptoms: psychomotor regression (dementia); seizures; Read More
Alopecia Cicatrisata (Pseudopelade) Pseudopelade is also known as Alopecia Cicatrisata. Pseudopelade is a very rare condition primarily affecting women and sometimes children. Read More
ACC (Aplasia Cutis Congenita) Aplasia cutis congenita (ACC) is a heterogenous group of disorders characterized by the absence of a portion of Read More
Acanthotic nevus Acanthotic nevus is an alternate name for seborrheic keratosis. It is a rare skin disease that consists of discolored lesions Read More
