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| CASE REPORT |
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| Year : 2016 |
Volume
: 27 | Issue : 1 | Page
: 100-102 |
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Bilateral cleft lip and palate, hypertelorism with agenesis of corpus callosum
SM Balaji
Director and Consultant, Balaji Dental and Craniofacial Hospital, Chennai, Tamil Nadu, India
Correspondence Address:
S M Balaji
Director and Consultant, Balaji Dental and Craniofacial Hospital, Chennai, Tamil Nadu
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0970-9290.179839
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Agenesis of corpus callosum (ACC) can have various development abnormalities spectrum. These include delay in milestones to complex neuropsychiatric manifestations. Following case report highlights the case of a young infant presenting with associated features including bilateral cleft lip and palate and hypertelorism. The kid was refused treatment at several centers owing to the central nervous system abnormality. This case reports highlight the ACC as a comorbid diagnosis in cleft lip and palate patient with hypertelorism perhaps owing to ignorance and fear of this apparently innocuous congenital malformation. |
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