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The skin weighs an average of four kilograms, covers an area of two square metres, and is made of three distinct layers: the epidermis, dermis, and subcutaneous tissue. [1] The two main types of human skin are: glabrous skin, the hairless skin on the palms and soles (also referred to as the "palmoplantar" surfaces), and hair-bearing skin. [3]
Chronic fatigue immune dysfunction syndrome. CFS. Chronic fatigue syndrome. CGBD. Corticobasal ganglionic degeneration. CH. Cluster headache. CHARGE syndrome. Coloboma of the eye, heart defects, atresia of the nasal choanae, retarded growth & or development, genital abnormalities, ear abnormalities.
This article provides a list of autoimmune diseases. These conditions, where the body's immune system mistakenly attacks its own cells, affect a range of organs and systems within the body. Each disorder is listed with the primary organ or body part that it affects and the associated autoantibodies that are typically found in people diagnosed ...
Skin condition. A skin condition, also known as cutaneous condition, is any medical condition that affects the integumentary system —the organ system that encloses the body and includes skin, nails, and related muscle and glands. [ 1] The major function of this system is as a barrier against the external environment. [ 2]
Printable version; Appearance. move to sidebar hide. This article has no lead section. Please improve this article by adding one in your own words. (August 2024) ...
Acne. What it looks like: Acne causes red, discolored bumps on the skin, along with whiteheads, blackheads, and cysts. Other symptoms to note: Acne is the most common skin condition affecting ...
Diseases of neonates and children younger than five years. Gonococcal ophthalmia neonatorum. Candida albicans infection. Candida parapsilosis infection. Cytomegalovirus infection. diphtheria. human coronavirus infection. respiratory distress syndrome. measles.
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.