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  2. Pfeiffer syndrome - Wikipedia

    en.wikipedia.org/wiki/Pfeiffer_syndrome

    Pfeiffer syndrome. Pfeiffer syndrome is a rare genetic disorder, characterized by the premature fusion of certain bones of the skull (craniosynostosis), which affects the shape of the head and face. The syndrome includes abnormalities of the hands and feet, such as wide and deviated thumbs and big toes. Pfeiffer syndrome is caused by mutations ...

  3. Marty Feldman - Wikipedia

    en.wikipedia.org/wiki/Marty_Feldman

    1968 Marty. Martin Alan Feldman (8 July 1934 [1] – 2 December 1982) was a British actor, comedian and comedy writer. He was known for his prominent, misaligned eyes. [2][3][4] He initially gained prominence as a writer with Barry Took on the ITV sitcom Bootsie and Snudge and the BBC Radio comedy programme Round the Horne.

  4. List of people with ME/CFS - Wikipedia

    en.wikipedia.org/wiki/List_of_people_with_ME/CFS

    YouTuber and science communicator. American. Merryn Crofts. Drama student whose death was caused by ME/CFS [18] British. Michael Crawford. Actor and singer. British. Mia Diekow [19]

  5. Crouzon syndrome - Wikipedia

    en.wikipedia.org/wiki/Crouzon_syndrome

    Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. Because the branchial arches are important developmental features in a growing embryo, disturbances in their development ...

  6. Mandy Sellars - Wikipedia

    en.wikipedia.org/wiki/Mandy_Sellars

    Mandy Sellars (born 20 February 1975 in Lancashire, United Kingdom) is a British woman with a rare genetic mutation that has resulted in extraordinary growth in both of her legs. In 2006, some doctors diagnosed Sellars as having Proteus syndrome, a very rare condition thought to affect only 120 people worldwide, [1] but more recent diagnoses ...

  7. Apert syndrome - Wikipedia

    en.wikipedia.org/wiki/Apert_syndrome

    Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified as a branchial arch syndrome, affecting the first branchial (or pharyngeal) arch, the precursor of the maxilla and mandible. Disturbances in the development of the branchial arches in fetal ...

  8. Pierre Robin sequence - Wikipedia

    en.wikipedia.org/wiki/Pierre_Robin_sequence

    Pierre Robin sequence [a] (/ p j ɛər r ɔː ˈ b æ̃ /; [3] abbreviated PRS) is a congenital defect observed in humans which is characterized by facial abnormalities.The three main features are micrognathia (abnormally small mandible), which causes glossoptosis (downwardly displaced or retracted tongue), which in turn causes breathing problems due to obstruction of the upper airway.

  9. Epstein–Barr virus - Wikipedia

    en.wikipedia.org/wiki/Epstein–Barr_virus

    The Epstein–Barr virus (EBV), formally called Human gammaherpesvirus 4, is one of the nine known human herpesvirus types in the herpes family, and is one of the most common viruses in humans. EBV is a double-stranded DNA virus. [2] Epstein–Barr virus (EBV) is the first identified oncogenic virus, that is a virus that can cause cancer.