## 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
GAPO syndrome: A new case
β Scribed by Sandgren, Gerd
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 396 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0148-7299
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π SIMILAR VOLUMES
GAPO syndrome in 2 sibs (brother and sister) and in a first cousin presented slight variations in the clinical picture. These include presence of some body hair, white eyelashes, deep furrows on sternum and back, disproportional body build, and minor skeletal abnormalities. It has been suggested tha
Recently, Marc ΒΈano and Richieri-Costa [1998] described a new autosomal dominant mandibulofacial dysostosis in a Brazilian family with five affected individuals, in three generation comprising malar hypoplasia, cleft lip with or without cleft palate, mild upslanting palpebral fissures, and abnormal