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The Woman with Hair But No Beard is a low deep-voiced associate of the Man with a Beard But No Hair where they are the latest members of Count Olaf's theatre troupe. Her "aura of menace" even frightens Count Olaf and Lemony Snicket states that he refused to write down her real name.
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.
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]
Poliosis. Depigmentation of sections of skin and hair in 48-year-old man with vitiligo and poliosis. Poliosis (also called poliosis circumscripta) is the decrease or absence of melanin (or colour) in head hair, eyebrows, eyelashes, or any other hirsute area. It is popularly known as white forelock when it affects hair directly above the forehead.
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.
Many autoimmune diseases can cause hair loss, including alopecia areata, lupus, thyroid diseases, and even psoriasis. Each disease affects your hair differently. Sometimes, your hair loss might ...
Changes in hair colour typically occur naturally as people age, eventually turning the hair grey and then white. This normally begins in the early to mid-twenties in men and late twenties in women. More than 60 percent of Americans have some grey hair by age 40. The age at which greying begins seems almost entirely due to genetics.
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.