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  2. Disappearing blonde gene - Wikipedia

    en.wikipedia.org/wiki/Disappearing_blonde_gene

    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.

  3. Uncombable hair syndrome - Wikipedia

    en.wikipedia.org/wiki/Uncombable_hair_syndrome

    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 ...

  4. Waardenburg syndrome - Wikipedia

    en.wikipedia.org/wiki/Waardenburg_syndrome

    Mutations in a single copy of SNAI2 have also been found to cause patches of hair depigmentation without any other symptoms. [25] Type 2E is caused by an autosomal dominant mutation in the gene SOX10. [4] Rarely, a mutation in a gene other than those currently known may be responsible for a Waardenburg syndrome with features of type 2.

  5. Ectodermal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Ectodermal_dysplasia

    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.

  6. Oculocutaneous albinism - Wikipedia

    en.wikipedia.org/wiki/Oculocutaneous_albinism

    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.

  7. Health Experts Debunk 4 Anti-Sunscreen Myths Spreading ... - AOL

    www.aol.com/health-experts-debunk-4-anti...

    This DNA damage can cause changes in your genes called mutations that lead to skin cancer,” he told Healthline. ... have blonde or red hair, have a history of excessive sun exposure, including ...

  8. Waardenburg syndrome type 1 - Wikipedia

    en.wikipedia.org/wiki/Waardenburg_Syndrome_Type_1

    PAX3 gene mutation Waardenburg syndrome type 1 is a congenital disorder that caused by a mutation in the PAX3 gene that results in abnormal development in the neural crest during early development. Type 1 results in early graying and white forelock and a notable distance between the eyes, noted as dystopia canthorum .

  9. Kaley Cuoco reveals she suddenly saw random man in her hotel ...

    www.aol.com/lifestyle/kaley-cuoco-reveals-she...

    Butt naked in my bathroom, in my shower, in my hotel room. So I'm really dramatically blow-drying my hair — it felt like I was in a commercial. And I look up. In the mirror, I see a man in my room."