Vitamin K deficiency is a form of avitaminosis resulting from insufficient vitamin K1 or vitamin K2 or both.
List of articles in "Disease" category - Page 150
Acute decompensated heart failure
Acute decompensated heart failure (ADHF) is a worsening of the symptoms typically shortness of breath (dyspnea) edema and fatigue in a patient with existing heart disease. ADHF is a common […]
Myocardial infarction
Myocardial infarction (from Latin: Infarctus myocardii MI) or acute myocardial infarction (AMI) is the medical term for an event commonly known as a heart attack. It happens when blood stops […]
Gynecomastia
Gynecomastia /ˌɡaɪnɨkɵˈmæstiə/ is a common condition characterized by the benign enlargement of breast tissue in males. It may occur transiently in newborns. Half or more of adolescent boys have some […]
High anion gap metabolic acidosis
High anion gap metabolic acidosis is a form of metabolic acidosis characterized by a high anion gapThe list of agents that cause high anion gap metabolic acidosis is similar to […]
Fetor
Generally a foul or unpleasant odor.In medical contexts fetor refers to an unpleasant odor emanating from an individual.Specific types include: fetor oris another term for halitosis fetor hepaticus uremic fetor […]
Pseudoporphyria
Pseudoporphyria (also known as Pseudoporphyria cutanea tarda) is a bullous photosensitivity that clinically and histologically mimics porphyria cutanea tarda. The difference is that no abnormalities in urine or serum porphyrin […]
FG syndrome
FG syndrome (FGS; also known as Opitz–Kaveggia syndrome) is a rare genetic syndrome linked to the X chromosome and causing physical anomalies and developmental delays. First reported by Opitz and […]
Thelaziasis
Thelaziasis (occasionally spelled thelaziosis) is the term for infestation with parasitic nematodes of the genus Thelazia. The adults of all Thelazia species discovered so far inhabit the eyes and associated […]
Urbach–Wiethe disease
Urbach–Wiethe disease (also known as lipoid proteinosis and hyalinosis cutis et mucosae) is a rare recessive genetic disorder with fewer than 300 reported cases since its discovery. It was first […]