Case Report: Two Newly Diagnosed Patients With KBG Syndrome-Two Different Molecular Changes
Mutations or deletions of ANKRD11 gene are responsible for the symptoms of KBG syndrome. The KBG syndrome is a rare genetic disorder which is inherited in an autosomal dominant manner. Affected patients usually have characteristic facial features, macrodontia of the upper central incisors, hand abno...
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| Main Authors: | , , , , |
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| Format: | Book |
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Frontiers Media S.A.,
2021-09-01T00:00:00Z.
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