molybdenum cofactor deficiency type a

Molybdenum Cofactor Deficiency Type A

Molybdenum cofactor deficiency type A (MoCD-A) is a rare autosomal recessive metabolic disorder that disrupts the function of molybdenum-dependent enzymes, particularly sulfite oxidase. This deficiency…
molluscum contagiosum infection

Molluscum Contagiosum Infection

Molluscum contagiosum is a viral skin infection caused by the Molluscum contagiosum virus (MCV), a member of the poxvirus family. It leads to small, raised,…
moderate to severe plaque psoriasis

Moderate to Severe Plaque Psoriasis

Moderate to severe plaque psoriasis is a chronic autoimmune skin disorder characterized by red, scaly plaques on the skin. This condition affects millions of people…
moderate persistent asthma

Moderate Persistent Asthma

Moderate persistent asthma is a chronic respiratory condition characterized by frequent symptoms, nighttime awakenings, and moderate airflow obstruction. Patients require daily medication and management strategies…
mixed intestinal helminthiasis

Mixed Intestinal Helminthiasis

Mixed intestinal helminthiasis refers to an infection caused by multiple species of parasitic worms, including nematodes (roundworms), cestodes (tapeworms), and trematodes (flukes). These parasites colonize…
mixed hyperlipidemia

Mixed Hyperlipidemia

Mixed hyperlipidemia is a metabolic disorder characterized by elevated levels of low-density lipoprotein (LDL) cholesterol, high triglycerides, and low levels of high-density lipoprotein (HDL) cholesterol.…
mixed epilepsy

Mixed Epilepsy

Mixed epilepsy is a neurological condition where an individual experiences both focal seizures and generalized seizures. Unlike specific epilepsy types that originate from one part…