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The shaft of normal hair (left) and hair in uncombable hair syndrome (right). The hair is normal in quantity and is usually silvery-blond or straw-colored. It is disorderly, stands out from the scalp, and cannot be combed flat, but it can be controlled by braiding methods. This is caused by mutations in one of three possible genes; PADI3, TGM ...
Blond hair is controlled by an allele that is recessive to most alleles responsible for darker hair, [1] but it is not a disappearing gene.. The "disappearing blonde gene" refers to a hoax that emerged in parts of the Western world in the early 2000s, claiming that a scientific study had estimated that blonds would become extinct within the next two centuries.
Canities subita, also called Marie Antoinette syndrome or Thomas More syndrome, is an alleged condition of hair turning white overnight due to stress or trauma. [1] The trivial names come from specific cases in history including that of Queen Marie Antoinette of France whose hair was noted as having turned stark white overnight after her capture following the ill-fated flight to Varennes ...
Diagnosing ED usually involves a clinical examination focused on core symptoms, such as lack of sweating, specific dental and hair abnormalities, and characteristic facial features. Genetic testing can confirm the diagnosis, especially when there is a family history of ED or when prenatal screening is considered.
It results in blonde hair and the eventual development of skin pigmentation during infancy, though at birth is difficult to distinguish from other types. [7] [11] About 1 in 40,000 people have some form of OCA1. [12] OCA2: 203200: OCA2: The most common type of albinism is caused by mutation of the P gene.
According to the sociologist Christie Davies, only around five percent of adults in Europe and North America are naturally blond. [42] A study conducted in 2003 concluded that only four percent of American adults are naturally blond. [43] A significant number of Caucasian women who have blonde hair have dyed it that way. [42] [44]
Werner syndrome patients exhibit growth retardation, short stature, premature graying of hair, alopecia (hair loss), wrinkling, prematurely aged faces with beaked noses, skin atrophy (wasting away) with scleroderma-like lesions, lipodystrophy (loss of fat tissues), abnormal fat deposition leading to thin legs and arms, and severe ulcerations around the Achilles tendon and malleoli (around ankles).
Other than its length, the hair shaft is normal. [4] Normal hair density. [4] Absence of fragility in hair. [4] When separating it from loose anagen syndrome or telogen effluvium, the hair pull test is frequently normal. [4] Normal physical exam (skin, teeth, and nails). [4] Average physical and mental growth. [4]