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GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva

Identifieur interne : 009E37 ( Main/Exploration ); précédent : 009E36; suivant : 009E38

GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva

Auteurs : Nagwa A. Meguid [Égypte] ; Hanan H. Afifi [Égypte] ; Magda I. Ramzy [Égypte] ; Amina Hindawy [Égypte] ; Samia A. Temtamy [Égypte]

Source :

RBID : ISTEX:9216BCB1BCBCC7F318221034890C7AD9FED31DCA

English descriptors

Abstract

We report on a 3‐year‐old boy with growth retardation, alopecia, pseudoanodontia, and optic atrophy. This is the 18th known and the first Egyptian case of GAPO syndrome. Electron microscopic examination of gingival biopsy showed excessive collagen fibres and endothelial vacuolisation, suggesting involvement of extracellular pathological collagenosis.

Url:
DOI: 10.1111/j.1399-0004.1997.tb02527.x


Affiliations:


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Le document en format XML

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<term>Biopsy</term>
<term>Deep parietal</term>
<term>Different families</term>
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<div type="abstract" xml:lang="en">We report on a 3‐year‐old boy with growth retardation, alopecia, pseudoanodontia, and optic atrophy. This is the 18th known and the first Egyptian case of GAPO syndrome. Electron microscopic examination of gingival biopsy showed excessive collagen fibres and endothelial vacuolisation, suggesting involvement of extracellular pathological collagenosis.</div>
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