Health Articles (Sorted by date)

Acinic cell carcinoma is a rare, low-grade malignant salivary gland neoplasm. These are malignant tumors of the salivary glands that are dervied from the salivary gland epithelium and characteristically forms glandular acini.

Acidemia propionic is an organic aciduria produced by the deficiency of propionyl CoA-carboxylase, producing a ketotic hyperglycinemia and recurrent metabolic imbalance.

Achondroplasia is an autosomal predominant disorder that is a popular reason of dwarfism. In achondroplasia, the mutated kind of the receptor is constitutively involved and this leads to seriously abbreviated bones.

Achalasia is a rare disease of the muscle of the esophagus. Achalasia, also known as esophageal achalasia, achalasia cardiae, cardiospasm, dyssynergia esophagus, and esophageal aperistalsis.

Aceruloplasminemia is an autosomal recessive disorder. It is characterized by liberal neurodegeneration of the retina and basal ganglia associated with particular inherited mutations in the ceruloplasmin gene.

Acanthosis nigricans is a disorder that may start at any age. It causes velvety, light-brown-to-black, markings normally on the neck, under the weaponry or in the groin. Acanthosis nigricans is almost frequently associated with obesity.

A syndrome characterized by a group of conditions that are considered leading danger factors for diabetes mellitus and cardiovascular disease. Metabolic syndrome is associated with abdominal obesity, blood lipid disorders, inflammation, insulin...

Cystic lymphangioma is a rare tumour, frequently situated in the cervical or axillary region and exceptionally intraabdominal. It is essentially a malformation of one of the abdominal lymph vessels where a portion is dilated and form a lymph...

An aneurysm is when a blood vessel becomes abnormally big or balloons outward. The precise reason is unidentified, but danger factors for developing an aortic aneurysm include higher blood force, smoking, higher cholesterol, obesity, emphysema,...

Afibrinogenemia is a occasional congenital blood disorder in which the blood does not coagulation normally due to a lack of or a malfunction involving fibrinogen, a protein necessary for coagulation.