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  2. File:Marfan Syndrome E00551 (CardioNetworks ECHOpedia).webm

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    What links here; Upload file; Special pages; Printable version; Page information

  3. Congenital contractural arachnodactyly - Wikipedia

    en.wikipedia.org/wiki/Congenital_contractural_ar...

    Congenital contractural arachnodactyly (CCA), also known as Beals–Hecht syndrome, is a rare autosomal dominant congenital connective tissue disorder. [1] As with Marfan syndrome, people with CCA typically have an arm span that is greater than their height and very long fingers and toes. [2]

  4. Marfan syndrome - Wikipedia

    en.wikipedia.org/wiki/Marfan_syndrome

    Marfan syndrome is treated by addressing each issue as it arises and, in particular, preventive medication even for young children to slow progression of aortic dilation. The goal of this treatment strategy is to slow the progression of aortic dilation and prevent any damage to heart valves by eliminating heart arrhythmias , minimizing the ...

  5. The Marfan Foundation - Wikipedia

    en.wikipedia.org/wiki/The_Marfan_Foundation

    The Foundation provides information about Marfan syndrome and funds research for the purposes of saving lives and improving the quality of life for people affected by the condition which is a genetic connective tissue disorder. The Foundation also lobbies Congress to fund Marfan syndrome research and engages in its own fundraising activities. [1]

  6. Dolichonychia - Wikipedia

    en.wikipedia.org/wiki/Dolichonychia

    Dolichonychia is a medical condition in which the nail beds of the fingers and toes are abnormally long and slender, specifically, a finger nail index of 1.30 or more, [1] it is a common feature in people with connective tissue disorders, such as Ehlers–Danlos syndromes, Marfan syndrome, and hypohidrotic ectodermal dysplasia., [2] it often appears alongside arachnodactyly and/or ...

  7. Today’s NYT ‘Strands’ Hints, Spangram and Answers for ...

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    Drag or tap letters to create words. If tapping, double tap the last letter to submit. Theme words fill the board entirely. No theme words overlap.

  8. 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 ...

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