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1.
Science ; 180(4082): 186-8, 1973 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-17811658

RESUMO

Cotton remains from four archeological sites in central coastal Peru, representing a time sequence from about 2500 to 1000 B.C., were compared with similar materials obtained from living wild and cultivated forms of Gossypium barbadense L. The comparison revealed that the archeological cotton samples were primitive forms of Gossypium barbadense, differing little from present-day wild forms of the same species. Although not the earliest cottons recorded for the New World, they appear to represent the earliest stages of cotton domestication yet recorded.

2.
Clin Radiol ; 53(4): 268-73, 1998 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9585042

RESUMO

Pendred syndrome comprises the association of severe congenital sensorineural deafness with thyroid pathology. Although it is the commonest form of syndromic hearing loss, the primary genetic defect remains unknown. The variable clinical presentation allied to the difficulty in securing the diagnosis have resulted in relatively poor documentation of the radiological features of this syndrome. We now present data on 40 patients, all complying with strict diagnostic criteria for the disorder, and describe our experience of the prevalence of specific malformations of the inner ear as well as comparing the relative merits of computed tomography (CT) and magnetic resonance imaging (MRI) in the investigation of this inherited condition. Deficiency of the interscalar septum in the distal coils of the cochlea (Mondini deformity) was found to be a common but probably not a constant feature of Pendred syndrome. However, enlargement of the endolymphatic sac and duct in association with a large vestibular aqueduct was present in all 20 patients examined by MRI. We conclude that thin section high resolution MRI on a T2 protocol in the axial and sagittal planes is the imaging investigation of choice.


Assuntos
Surdez/diagnóstico por imagem , Orelha Interna/anormalidades , Cóclea/anormalidades , Cóclea/diagnóstico por imagem , Surdez/congênito , Orelha Interna/diagnóstico por imagem , Orelha Interna/patologia , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Síndrome , Tomografia Computadorizada por Raios X , Vestíbulo do Labirinto/anormalidades , Vestíbulo do Labirinto/patologia
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