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  2. Marfan syndrome - Wikipedia

    en.wikipedia.org/wiki/Marfan_syndrome

    Marfan syndrome is named after Antoine Marfan, [11] the French pediatrician who first described the condition in 1896 after noticing striking features in a five-year-old girl. [ 12 ] [ 77 ] The gene linked to the disease was first identified by Francesco Ramirez at the Mount Sinai Medical Center in New York City in 1991.

  3. 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.

  4. Multiple endocrine neoplasia type 2B - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine...

    Unlike Marfan syndrome, the cardiovascular system and the lens of the eye are unaffected. [citation needed] Mucosal neuromas are the most consistent and distinctive feature, appearing in 100% of patients. [11] Usually there are numerous yellowish-white, sessile, painless nodules on the lips or tongue, with deeper lesions having normal coloration.

  5. 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] [5] These features include a tall, thin stature and long, slender limbs. [5]

  6. Ehlers–Danlos syndrome - Wikipedia

    en.wikipedia.org/wiki/Ehlers–Danlos_syndrome

    Several disorders share some characteristics with EDS. For example, in cutis laxa, the skin is loose, hanging, and wrinkled. In EDS, the skin can be pulled away from the body, but is elastic and returns to normal when let go. In Marfan syndrome, the joints are very mobile, and

  7. Facies (medical) - Wikipedia

    en.wikipedia.org/wiki/Facies_(medical)

    Pitt–Hopkins syndrome; Beta thalassemia is associated with distinctive facial features due to ineffective erythropoiesis. The ineffective erythropoiesis causes marrow hyperplasia or expansion and bony changes, including the bones of the face; this causes craniofacial protrusions.

  8. Don't try to categorize Khruangbin, just absorb the Grammy ...

    www.aol.com/dont-try-categorize-khruangbin-just...

    The name − pronounced KRUNG-bin− is Thai for airplane. Appropriately, the group's music often lifts you to a somewhat liminal state, swaying between altitudes and time zones.

  9. Arachnodactyly - Wikipedia

    en.wikipedia.org/wiki/Arachnodactyly

    This feature can occur on its own with no underlying health problems, or it can be associated with certain medical conditions, including Marfan syndrome, [1] Ehlers–Danlos syndromes, [2] Loeys–Dietz syndrome, and homocystinuria. [3]