OspA heterogeneity of Borrelia valaisianaconfirmed by phenotypic and genotypic analyses

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منابع مشابه

OspA heterogeneity of Borrelia valaisiana confirmed by phenotypic and genotypic analyses

BACKGROUND Although European Borrelia burgdorferi sensu lato isolates have been divided into five genospecies, specific tools for the serotype characterization of only three genospecies are available. Monoclonals antibodies (mAbs) H3TS, D6 and I17.3 identify B. burgdorferi sensu stricto (ss.), B. garinii and B. afzelii respectively, but no mAbs are available to identify B. valaisiana. In the sa...

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Genotypic and phenotypic heterogeneity in familial microcoria.

AIMS To describe the clinical features and genetic findings in two families presenting with microcoria inherited as an autosomal dominant trait. METHODS Both affected and unaffected members of two families displaying familial microcoria were examined. Flash photography or infrared pupillography were used to assess pupils, and a full ophthalmic examination including visual acuity and field tes...

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Genotypic and phenotypic analyses of Korean patients with syndromic craniosynostosis.

To the Editor : Craniosynostosis, the premature fusion of one or more cranial sutures, is a common malformation occurring in approximately 1 in 2500 live births (1), and ocular hypertelorism, proptosis, beaking of the nose and midface hypoplasia are the common facial features of the craniosynostosis (2, 3). The syndromic craniosynostosis is the hereditary form of craniosynostosis, which is asso...

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Phenotypic and genotypic heterogeneity in familial Milroy lymphedema.

Familial Milroy lymphedema (ML) is classified as an autosomal dominant disorder characterized by peripheral edema of the lower extremities at birth or in early childhood. The variety of phenotypes are not well described, and the genomic location and functional expression of the gene or genes underlying this and related familial lymphedema syndromes remain largely unknown. In this collaborative ...

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SCIENTIFIC REPORT Genotypic and phenotypic heterogeneity in familial microcoria

Aims: To describe the clinical features and genetic findings in two families presenting with microcoria inherited as an autosomal dominant trait. Methods: Both affected and unaffected members of two families displaying familial microcoria were examined. Flash photography or infrared pupillography were used to assess pupils, and a full ophthalmic examination including visual acuity and field tes...

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ژورنال

عنوان ژورنال: BMC Infectious Diseases

سال: 2003

ISSN: 1471-2334

DOI: 10.1186/1471-2334-3-14