To understand the aqueous species important for transport of rhenium under supercritical conditions, we conducted a series of solubility experiments on the Re–ReO2 buffer assemblage and ReS2. In these experiments, pH was buffered by the K–feldspar–muscovite–quartz assemblage; fO2 in sulfur-free systems was buffered by the Re–ReO2 assemblage; and fO2 and fS2 in sulfur-containing systems were buf...

INTRODUCTION Treacher Collins syndrome is an autosomal dominant disorder resulting in congenital craniofacial deformities. Scoliosis has not been previously reported as one of the extracranial manifestations of this syndromic condition. CASE PRESENTATION We present a 15-year-old British Caucasian girl with Treacher Collins syndrome who developed a severe double thoracic scoliosis measuring 10...

Treacher Collins syndrome is a congenital disorder with bilaterally symmetric anomalies of the structures developing from the first and second branchial arches. The ocular and orbital features are an obligatory component for the diagnosis. We presented a case of typical, complete syndrome and also reviewed the varied ophthalmological manifestations of the disease in the literature. Antimongoloi...

Mr. Eason in the July number of the Lancet, 1911, writes a paper on Cataract Extraction, the basis of which is not his own personal experience but a paper published in the Royal London Ophthalmic Hospital Reports, Volume 16, Part 3, October 1905, by Mr. E. Treacher Collins and a paper by Mr. Charles Higgins {Lancet, 13th April 1907), and a paper published by Major Kilkelly in the Indian Medical...

Treacher-Collins syndrome (TCS) is a rare dominant autosomal anomaly resulting from malformation or disruption of the development of the first and second branchial arches. It is characterized by micrognathia, malar hypoplasia, and malformations of the eyes and ears. The prenatal diagnosis using two-dimensional ultrasonography (2DUS) is characterized by identification of facial malformations tog...