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| Year : 1997 | Volume
: 45
| Issue : 1 | Page : 34--37 |
Oral facial digital syndrome.
Z Hussain, K Logamuthukrishnan, S Dharmarajan, G Thiagarajan, SD Subbaiah, GSJ Narayana, M Anbuselvam
, L Murugan, S Pugazhendhi
Department of Neurology, Government General Hospital, Madras - 600 003, India
Correspondence Address:
Z Hussain
Department of Neurology, Government General Hospital, Madras - 600 003
India
 Source of Support: None, Conflict of Interest: None  | Check |
PMID: 29509158 
We report a female infant with features suggestive of Oral Facial Digital Syndrome (OFDS) Type I and associated cerebellar anomalies with Dandy-Walker malformation which suggest OFDS Type VI. The phenotypic overlap in this child OFDS type I and TypeVI raises the question as to whether they represent separate genetic entities. This pattern of abnormalities appears to be unique.
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