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  2. Marfanoid - Wikipedia

    en.wikipedia.org/wiki/Marfanoid

    Marfanoid (or Marfanoid habitus) is a constellation of signs resembling those of Marfan syndrome, including long limbs, with an arm span that is at least 1.03 of the height of the individual, and a crowded oral maxilla, sometimes with a high arch in the palate, arachnodactyly, and hyperlaxity.

  3. Lujan–Fryns syndrome - Wikipedia

    en.wikipedia.org/wiki/Lujan–Fryns_syndrome

    Lujan–Fryns syndrome (LFS) is an X-linked genetic disorder that causes mild to moderate intellectual disability and features described as Marfanoid habitus, referring to a group of physical characteristics similar to those found in Marfan syndrome.

  4. Marfan syndrome - Wikipedia

    en.wikipedia.org/wiki/Marfan_syndrome

    Marfanoid–progeroid–lipodystrophy syndrome (MPL), also referred to as Marfan lipodystrophy syndrome (MFLS), is a variant of MFS in which Marfan symptoms are accompanied by features usually associated with neonatal progeroid syndrome (also referred to as Wiedemann–Rautenstrauch syndrome) in which the levels of white adipose tissue are ...

  5. Malouf syndrome - Wikipedia

    en.wikipedia.org/wiki/Malouf_syndrome

    Malouf syndrome (also known as "congestive cardiomyopathy-hypergonadotropic hypogonadism syndrome") is a congenital disorder that causes one or more of the following symptoms: intellectual disability, ovarian dysgenesis, congestive cardiomyopathy, broad nasal base, blepharoptosis, and bone abnormalities, and occasionally marfanoid habitus (tall stature with long and thin limbs, little ...

  6. Marfanoid–progeroid–lipodystrophy syndrome - Wikipedia

    en.wikipedia.org/wiki/Marfanoid–progeroid...

    Marfanoid–progeroid–lipodystrophy syndrome (MPL), also known as Marfan lipodystrophy syndrome (MFLS) or progeroid fibrillinopathy, is an extremely rare medical condition which manifests as a variety of symptoms including those usually associated with Marfan syndrome, an appearance resembling that seen in neonatal progeroid syndrome (NPS; also known as Wiedemann–Rautenstrauch syndrome ...

  7. Ehlers–Danlos syndrome - Wikipedia

    en.wikipedia.org/wiki/Ehlers–Danlos_syndrome

    Other common features include a "marfanoid habitus" characterized by long, slender fingers (arachnodactyly), unusually long limbs, and a sunken chest (pectus excavatum) or protruding chest (pectus carinatum). [5] It can be caused by variations in the gene PLOD1, or rarely, in the FKBP14 gene. [33]

  8. Morgan Fairchild then and now: She's still glamorous as ever ...

    www.aol.com/entertainment/morgan-fairchild-then...

    Today, Fairchild is 69 -- although you wouldn't know it from photos! In the last decade, she's appeared on countless TV shows, from "Two and a Half Men" to "My Name Is Earl" and, most recently ...

  9. Multiple endocrine neoplasia - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine_neoplasia

    Multiple endocrine neoplasia (abbreviated MEN) is a condition which encompasses several distinct syndromes featuring tumors of endocrine glands, each with its own characteristic pattern.