1 jan 2018 · KBG syndrome is a rare disorder that affects several body systems. Explore symptoms, inheritance, genetics of this condition.
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What is a KBG?
What are the symptoms of KGB?
What is the diagnosis KGB?
What are the behaviors of KBG syndrome?
Disease Overview. KBG syndrome (KBGS) is a rare genetic disorder characterized by large front teeth (macrodontia), characteristic facial features, ...
KBG syndrome is a rare condition characterised by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) ...
A rare congenital malformation syndrome characterized by a typical facial dysmorphism, macrodontia of the permanent upper central incisors, short stature, ...
22 mrt 2018 · KBG syndrome is typically characterized by macrodontia (especially of the upper central incisors), characteristic facial features ...
KBG syndrome is a rare genetic disease that is the result of a mutation in the ANKRD11 gene at location 16q24.3. Only about a hundred known cases have been ...
19 dec 2017 · KBG syndrome is a rare genetic disorder characterized by macrodontia of upper permanent incisors, distinctive craniofacial features, skeletal ...
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.
