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Laryngopyocele: three new clinical cases and review of the literature

✍ Scribed by L. Cassano; P. Lombardo; R. M. Ragona; A. Pastore


Publisher
Springer-Verlag
Year
2000
Tongue
English
Weight
94 KB
Volume
257
Category
Article
ISSN
0302-9530

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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