A RARE CASE OF SHPRINTZEN GOLDBERG SYNDROME
Journal Title: Journal of Evolution of Medical and Dental Sciences - Year 2016, Vol 5, Issue 18
Abstract
The Shprintzen-Goldberg syndrome is very rare with fewer than fifty cases described in the medical literature to date. Here, we present a 12-year male child with craniosynostosis along with Marfanoid features with skeletal and neurological abnormalities. It is a multiple anomaly syndrome that affects many parts of the body
Authors and Affiliations
Ingle , Prashant , Priyanka
Keywords
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- EP ID EP123301
- DOI 10.14260/jemds/2016/212
- Views 89
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