Apert syndrome variant with overlapping features of Crouzon syndrome.
Article
in English
| IMSEAR
| ID: sea-86162
ABSTRACT
A rare variant of Apert syndrome having overlapping features of Crouzon syndrome is described. The salient features of the two syndromes are briefly discussed and overlapping features are highlighted. A possible genetic explanation for the same is mentioned.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Acrocephalosyndactylia
/
Humans
/
Male
/
Tomography, X-Ray Computed
/
Cerebral Ventricles
/
Adult
/
Craniofacial Dysostosis
/
Diagnosis, Differential
/
India
Type of study:
Diagnostic study
Country/Region as subject:
Asia
Language:
English
Year:
2000
Type:
Article
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