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  2. Full Service (book) - Wikipedia

    en.wikipedia.org/wiki/Full_Service_(book)

    978-0-8021-2007-6. Full Service: My Adventures in Hollywood and the Secret Sex Lives of the Stars is a 2012 "tell-all" book about the sex lives of Hollywood stars from the late 1940s to the early 1980s by Scotty Bowers, with Lionel Friedberg as a contributing author. Bowers makes many claims about the sex lives of many people, most of whom were ...

  3. Weaver syndrome - Wikipedia

    en.wikipedia.org/wiki/Weaver_syndrome

    Weaver syndrome is an extremely rare autosomal dominant genetic disorder associated with rapid growth beginning in the prenatal period and continuing through the toddler and youth years. It is characterized by advanced osseous maturation and distinctive craniofacial, skeletal and neurological abnormalities. [1]

  4. Marshall–Smith syndrome - Wikipedia

    en.wikipedia.org/wiki/Marshall–Smith_syndrome

    Marshall-Smith Syndrome, discovered in 1971 (Marshall, Graham, Scott, Boner, & Smith), is characterized by unusual accelerated skeletal maturation (usually starting before birth) and symptoms like conspicuous physical characteristics, respiratory difficulties, and mental retardation. Cases described in the literature show a clinical variability ...

  5. Will Weaver - Wikipedia

    en.wikipedia.org/wiki/Will_Weaver

    Weaver has also written many stories for young adults, including the Billy Baggs baseball novels. These include Striking Out, Farm Team, and Hard Ball. He has also written Memory Boy, Claws, Full Service, and Defect. Saturday Night Dirt, the first of a series on dirt-racers, was released in 2008 followed by Super Stock Rookie.

  6. Williams syndrome - Wikipedia

    en.wikipedia.org/wiki/Williams_syndrome

    1 in 20,000 to 1 in 7,500 [4] Williams syndrome ( WS ), also Williams–Beuren syndrome ( WBS ), is a genetic disorder that affects many parts of the body. [2] Facial features frequently include a broad forehead, underdeveloped chin, short nose, and full cheeks. [2] Mild to moderate intellectual disability is observed in people with WS, with ...

  7. Prader–Willi syndrome - Wikipedia

    en.wikipedia.org/wiki/Prader–Willi_syndrome

    1 in 15,000–20,000 people [2] Prader–Willi syndrome ( PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. [2] In newborns, symptoms include weak muscles, poor feeding, and slow development. [2] Beginning in childhood, those affected become constantly hungry, which often leads to obesity and type ...

  8. Beckwith–Wiedemann syndrome - Wikipedia

    en.wikipedia.org/wiki/Beckwith–Wiedemann_syndrome

    Beckwith–Wiedemann syndrome (/ ˈ b ɛ k ˌ w ɪ θ ˈ v iː d ə. m ə n /; abbreviated BWS) is an overgrowth disorder usually present at birth, characterized by an increased risk of childhood cancer and certain congenital features. A minority (<15%) of cases of BWS are familial, meaning that a close relative may also have BWS, and parents ...

  9. Smith–Magenis syndrome - Wikipedia

    en.wikipedia.org/wiki/Smith–Magenis_syndrome

    Smith–Magenis syndrome (SMS), also known as 17p- syndrome, is a microdeletion syndrome characterized by an abnormality in the short (p) arm of chromosome 17. It has features including intellectual disability, facial abnormalities, difficulty sleeping, and numerous behavioral problems such as self-harm. Smith–Magenis syndrome affects an ...