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tick bites, e.g. Ixodes scapularis. Balantidiasis. Balantidium coli. intestinal mucosa, may become invasive in some patients. stool (diarrhea=ciliated trophozoite; solid stool=large cyst with horseshoe shaped nucleus) ingestion of cyst, zoonotic infection acquired from pigs (feces) Blastocystosis. Blastocystis spp.
List of autoimmune diseases. Dermatosis in Crohn's disease. Demyelination in MS. PAS stain of lupus nephritis. Autoimmune urticaria. Proptosis in Graves' disease. 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 ...
Melanoacanthoma (pigmented seborrheic keratosis) Merkel cell carcinoma (cutaneous apudoma, primary neuroendocrine carcinoma of the skin, primary small cell carcinoma of the skin, trabecular carcinoma of the skin) Microcystic adnexal carcinoma (sclerosing sweat duct carcinoma) Micronodular basal cell carcinoma.
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.
Albinism is a congenital condition characterized in humans by the partial or complete absence of pigment in the skin, hair and eyes. Albinism is associated with a number of vision defects, such as photophobia, nystagmus, and amblyopia. Lack of skin pigmentation makes for more susceptibility to sunburn and skin cancers.
Uncombable hair syndrome ( UHS) is a rare structural anomaly of the hair with a variable degree of effect. It is characterized by hair that is silvery, dry, frizzy, wiry, and impossible to comb. [ 4] It was first reported in the early 20th century. [ 5] It typically becomes apparent between the ages of 3 months and 12 years. [ 6]
Medical genetics. Hair diseases are illnesses that impact the persistence and regular growth of hair. Types of hair diseases include folliculitis, hirsutism, hypertrichosis, hypotrichosis ( alopecia ), Menkes kinky hair syndrome, monilethrix, and piedra. [ 1]
Netherton syndrome is an autosomal recessive disorder associated with mutations in the SPINK5 gene, which encodes the serine protease inhibitor lympho-epithelial Kazal-type-related inhibitor ( LEKTI ). [ 2] These mutations result in a dysfunctional protein that has a reduced capacity to inhibit serine proteases expressed in the skin.