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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

    Uncombable hair syndrome 2 is caused by a defect in transglutaminase 3 (TGM3) gene. This gene helps provide instructions for creating an enzyme known as transglutaminase 3. This gene is found in skin cells known as keratinocytes and corneocytes. This helps frame the scalp, root, and strands of hair. [14] It helps the molecules bind to other ...

  4. Waardenburg syndrome - Wikipedia

    en.wikipedia.org/wiki/Waardenburg_syndrome

    Rarely, a mutation in a gene other than those currently known may be responsible for a Waardenburg syndrome with features of type 2. This is usually initially classified as simply type 2 but may be given its own subtype once a gene or locus is identified and established. [7] Type 3 is caused by a mutation in the gene PAX3, the same gene as in ...

  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. Poliosis - Wikipedia

    en.wikipedia.org/wiki/Poliosis

    Poliosis circumscripta, commonly referred to as a "white forelock", is a condition characterized by localized patches of white hair due to a reduction or absence of melanin in hair follicles. Although traditionally associated with the scalp, poliosis can affect any hairy area on the body, including eyebrows, eyelashes, and beards.

  8. Ellen DeGeneres Ditches Signature Blonde Hair as She's ... - AOL

    www.aol.com/ellen-degeneres-ditches-signature...

    DeGeneres' lifestyle change comes two years afterThe Ellen DeGeneres Show, which aired for 19 seasons, aired its final episode in May 2022.The show came to a close following toxic workplace ...

  9. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    P – Point mutation, or any insertion/deletion entirely inside one gene; D – Deletion of a gene or genes; Dup - Duplication of a gene or genes; C – Whole chromosome extra, missing, or both (see chromosome abnormality) T – Trinucleotide repeat disorders: gene is extended in length