KBG syndrome: 16q24.3 microdeletion in an Indian patient.


Introduction KBG syndrome (OMIM No. 148 050) is characterized by macrodontia of the upper central incisors, distinctive craniofacial findings, short stature, skeletal anomalies, wide and arched eyebrows, and neurologic involvement that includes global developmental delay, seizures, and intellectual disability (Sirmaci et al., 2011). Since 1975, more than 70… (More)
DOI: 10.1097/MCD.0000000000000168


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