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Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature

✍ Scribed by Boerkoel, C. F.; O'Neill, S.; André, J. L.; Benke, P. J.; Bogdanovíć, R.; Bulla, M.; Burguet, A.; Cockfield, S.; Cordeiro, I.; Ehrich, J. H. H.


Book ID
113042806
Publisher
Springer
Year
2000
Tongue
English
Weight
181 KB
Volume
159
Category
Article
ISSN
0340-6997

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## Abstract The GAPO syndrome is an extremely rare autosomal recessive disease that presents as main characteristics evident growth retardation, alopecia, pseudoanodontia, progressive optic atrophy and a typical face. Until now, only 30 patients have been reported in the medical literature (nine of