A de novo Microdeletion of ANKRD11 Gene in a Korean Patient with KBG Syndrome
Annals of Laboratory Medicine
;
: 390-394, 2014.
Artículo
en Inglés
| WPRIM
| ID: wpr-216382
ABSTRACT
KBG syndrome is a very rare genetic disorder characterized by macrodontia of upper central incisors, global developmental delay, distinctive craniofacial features, short stature, and skeletal anomalies. Ankyrin repeat domain 11 gene (ANKRD11) has recently been identified as a causal factor of this syndrome. We describe a 6-yr-old Korean boy with features of KBG syndrome. The patient had a short stature, macrodontia, dysmorphic facial features, speech and motor delay with intellectual disability, and partial seizures as indicated by the electroencephalogram, but he was neither autistic nor had autism spectrum disorders. Using high-resolution oligonucleotide array comparative genomic hybridization, we identified a heterozygous 240-kb deletion at 16q24.3 corresponding to ANKRD11. This patient provided additional evidence on the influence of ANKRD11 in KBG syndrome and suggested that deletion limited to ANKRD11 is unlikely to cause autism.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Fenotipo
/
Proteínas Represoras
/
Anomalías Dentarias
/
Anomalías Múltiples
/
Enfermedades del Desarrollo Óseo
/
Cromosomas Humanos Par 16
/
Eliminación de Gen
/
Facies
/
Pueblo Asiatico
/
Electroencefalografía
Tipo de estudio:
Estudio pronóstico
Límite:
Niño
/
Humanos
/
Masculino
País/Región como asunto:
Asia
Idioma:
Inglés
Revista:
Annals of Laboratory Medicine
Año:
2014
Tipo del documento:
Artículo
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