Partial Deletion Of Ankrd11 Results In The Kbg Phenotype Distinct From The 16q24.3 Microdeletion Syndrome
Title
Partial Deletion Of Ankrd11 Results In The Kbg Phenotype Distinct From The 16q24.3 Microdeletion Syndrome
Creator
Khalifa M; Stein J; Grau L; Nelson V; Meck J; Aradhya S; Duby J
Publisher
American Journal of Medical Genetics Part A
Date
2013
2013-04
Description
KBG syndrome (OMIM 148050) is a very rare genetic disorder characterized by macrodontia, distinctive craniofacial abnormalities, short stature, intellectual disability, skeletal, and neurologic involvement. Approximately 60 patients have been reported since it was first described in 1975. Recently mutations in ANKRD11 have been documented in patients with KBG syndrome, and it has been proposed that haploinsufficiency of ANKRD11 is the cause of this syndrome. In addition, copy number variation in the 16q24.3 region that includes ANKRD11 results in a variable phenotype that overlaps with KBG syndrome and also includes autism spectrum disorders and other dysmorphic facial features. In this report we present a 21/2-year-old African American male with features highly suggestive of KBG syndrome. Genomic microarray identified an intragenic 154kb deletion at 16q24.3 within ANKRD11. This child's mother was mosaic for the same deletion (present in approximately 38% of cells) and exhibited a milder phenotype including macrodontia, short stature and brachydactyly. This family provides additional evidence that ANKRD11 causes KBG syndrome, and the mild phenotype in the mosaic form suggests that KBG phenotypes might be dose dependent, differentiating it from the more variable 16q24.3 microdeletion syndrome. This family has additional features that might expand the phenotype of KBG syndrome. (c) 2013 Wiley Periodicals, Inc.
Subject
16q24; 3; ANKRD11; ASD; autism; delineation; diagnostic-criteria; Genetics & Heredity; KBG; macrodontia; MCA; microdeletion; mosaicism; MR
Identifier
Format
Journal Article or Conference Abstract Publication
URL Address
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Pages
835-840
Issue
4
Volume
161A
Citation
Khalifa M; Stein J; Grau L; Nelson V; Meck J; Aradhya S; Duby J, “Partial Deletion Of Ankrd11 Results In The Kbg Phenotype Distinct From The 16q24.3 Microdeletion Syndrome,” NEOMED Bibliography Database, accessed October 14, 2024, https://neomed.omeka.net/items/show/10455.