BACKGROUND: Binder syndrome is a maxillonasal dysostosis characterized by midface and nasal hypoplasia, sometimes associated with short terminal phalanges of fingers and toes and transient radiological features of chondrodysplasia punctata. Warfarin-or phenytoin-induced vitamin K deficiency during e
Prenatal exposure to phenytoin, facial development, and a possible role for vitamin K
β Scribed by Howe, Andrew M. ;Lipson, Anthony H. ;Sheffield, Leslie J. ;Haan, Eric A. ;Halliday, Jane L. ;Jenson, Fred ;David, David J. ;Webster, William S.
- Book ID
- 102701588
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 785 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0148-7299
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β¦ Synopsis
Ten patients with maxillonasal hypoplasia (Binder "syndrome"), who were prenatally exposed to phenytoin (usually in combination with other anticonvulsants), were identified retrospectively. In addition to their facial anomalies, 6 of the patients were radiographed neonatally and showed punctate calcification, characteristic of chondrodysplasia punctata. Evidence is presented that the facial abnormalities seen in these children are due to anticonvulsant-induced vitamin K deficiency, causing abnormal development of the cartilaginous nasal septum. We propose that early vitamin K supplementation of at-risk pregnancies may prevent the development of maxillonasal hypoplasia, which in some patients is severely disfiguring and causes great emotional distress. Correction of this facial defect requires surgical and dental treatment over a long period of time.
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