Accutane Embryopathy Accutane embryopathy is a rare disorder and it is also called as Fetal Retinoid Syndrome. Accutane Embryopathy is a characteristic pattern of mental and physical birth d… Read More
Accessory Atrioventricular Pathways By definition, accessory atrioventricular pathways are aberrant muscle bundles that connect the atrium to a ventricle outside of the regular atrioventricu… Read More
Agammaglobulinemia Agammaglobulinemia, or hypogammaglobulinemia, is the most common of the primary immunodeficiencies, accounting for approximately 50% of cases. Three major types can be des… Read More
Congenital Afibrinogenemia Congenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to the lack of fibrinogen, a bl… 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 char… Read More
Alpers Disease Alpers disease is a progressive, neurodevelopmental, mitochondrial DNA depletion syndrome characterized by three co-occurring clinical symptoms: psychomotor regression (dement… Read More
Alopecia Cicatrisata (Pseudopelade) Pseudopelade is also known as Alopecia Cicatrisata. Pseudopelade is a very rare condition primarily affecting women and sometimes children. Initially, Pse… Read More
ACC (Aplasia Cutis Congenita) Aplasia cutis congenita (ACC) is a heterogenous group of disorders characterized by the absence of a portion of skin in a localized or widespread area at birth… Read More
Alopecia Celsi Alopecia areata is a disorder characterized by loss of hair. Sometimes, this means simply a few bare patches on the scalp. In other cases, hair loss is more extensive. Althoug… Read More
Acanthotic nevus Acanthotic nevus is an alternate name for seborrheic keratosis. It is a rare skin disease that consists of discolored lesions that appear to be oily. Since these lesions see… Read More
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