Gergely Balaton

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Cleidocranial dysplasia (CCD) is an uncommon, generalized skeletal disorder characterized by delayed ossification of the skull, aplastic or hypoplastic clavicles, and serious, complex dental abnormalities. There are many difficulties in the early diagnosis of CCD because a majority of the craniofacial abnormalities becomes obvious only during adolescence.(More)
Williams–Beuren syndrome (WS) is a genetic condition with an incidence of 1 in 20,000–50,000 live births. The syndrome consists of supravalvular aortic stenosis, characteristic dysmorphic facial features named “elf face” and intellectual disability. Early diagnosis of the syndrome is important since many of its features require treatment, and the prognosis(More)
HINTERGRUND: Das Williams-Beuren-Syndrom (WBS) ist ein mehrere Organsystem betreffender Entwicklungsschaden, der durch eine Mikrodeletion am Chromosom 7q11.23 bedingt ist. In seiner klassischen Form präsentiert es sich mit dysmorphen Gesichtszügen, mit Gelenkskontrakturen, mit Wachstums-und mentaler Retardation, mit räumlichen und visuellen kognitiven(More)
A 24-year-old male with red tattoos developed ocular pain and blurred vision three years after having been tattooed. The patient also noticed redness and itching in the area of the tattooed skin (Fig. 1). The rest of the history and physical examination was unremarkable. Routine laboratory screening tests were within normal limits, with the exception of a(More)
AIMS The currently licensed seasonal trivalent influenza vaccines contain 15 μg haemagglutinin per strain for adult, and up to 60 μg for elderly patients. However, due to recent shortages, dose sparing to increase production capacity would be highly desirable. In the present study, we attempted to find a dose-response relationship for immunogenicity and,(More)
Our study is aimed to focus on severe hypodontia, the absence of multiple teeth in permanent dentition. Examining the variation of the number of teeth agenesis of permanent teeth is relatively common but real oligodontia is rarely encountered during our daily work. At a number of patients recently attending the Pedodontics and Orthodontics Department of the(More)
A cleidocranial dysplasia is an autosomal dominant inherited condition consisting of generalized skeletal disorder. Associated dental signs are present in 93,5%; failure of tooth eruption with multiple supernumerary teeth, dilaceration of roots, crown germination, microdontia, high arched palate, midface hypoplasia, high gonion angle. The molecular- genetic(More)
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