The Official KBG syndrome awareness ribbon and associated designs are downloadable for your private use. If you choose to use any of the graphics for fundraising you must first fill out a request for use form.

KBG Syndrome is a rare genetic syndrome that can affect anyone but generally shows up in childhood. Learn more about how it can affect you or your child. Look—we know it can be hard to hear that you or your child has KBG Syndrome. You probably feel overwhelmed and confused. You're asking yourself, “What now?” Patient Registry!

KBG syndrome is a neurodevelopmental autosomal dominant disorder characterized by short stature, macrodontia, developmental delay, behavioral problems, speech delay and delayed closing of...

These documents are all free for personal use or to share with others about KBG Syndrome. If you would like to use them for any other reason please reach out to us at [email protected].

2023年8月15日 · KBG syndrome (KBGS) is a rare genetic disorder characterized by large front teeth (macrodontia), characteristic facial features, short to normal stature, developmental delay or intellectual disability (the level of intellectual disability is usually mild, and there are also people with KBGS who have a normal development).

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KBG syndrome is a rare condition characterized mainly by skeletal abnormalities, distinctive facial features, and intellectual disability. Specific signs and symptoms may include delayed bone age; abnormalities of the bones of the spine, ribs, and/or hands; large teeth (macrodontia); short stature; developmental delay; and behavioral or ...

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KBG syndrome is a rare genetic disease that is the result of a mutation in the ANKRD11 gene at location 16q24.3. [1] Only about a hundred known cases have been reported, although it is expected to be under-reported. The syndrome was first described by Herrmann in 1975 in three distinct families. [2]

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