The content of various phosphorus forms in sediments and the content of iron in interstitial waters were measured in sediment samples collected in the Gulf of Gdansk in March 2001. The studies showed that the greatest amounts of the total phosphorus and total dissolved iron were present in the uppermost sediment layer, and their respective concentrations ranged from 203,99 mumol?g-1d.w. to 1894,02 mumol?g-1d.w., and from 0,02 mumol?dm-3 to 4,68 mumol?dm-3. The contents of these parameters were directly connected with the type of sediment - the greatest concentrations were measured in fine sediments. The analysis of multiple correlation coefficients demonstrated that in over 90% of cases the concentration of phosphorus bound with iron depended on: the sediment type and its humidity, the content of organic matter, and the concentration of the total iron dissolved in the interstitial waters.
We report on a 2-year-old Polish girl with typical manifestations of Loeys-Dietz syndrome (LDS), a rare genetic condition belonging to the group of Marfan-related disorders. The characteristic LDS symptoms observed in the girl included craniofacial dysmorphism (craniosynostosis, cleft palate, hypertelorism), arachnodactyly, camptodactyly, scoliosis, joint laxity, talipes equinovarus, translucent and hyperelastic skin, and umbilical hernia. Mild dilatation of the ascending aorta and tortuous course of the left internal carotid artery were recognized during her second year of life. Molecular genetic testing revealed a heterozygous missense mutation (c.1582C>T, p.R528C) in the transforming growth factor beta receptor II gene (TGFBR2). This mutation has been previously associated with LDS in 5 unrelated cases, and was never reported in patients with other Marfan-related disorders. Comparison of the phenotypes of our patient and these 5 individuals with c.1582C>T showed that only the hallmark triad of the syndrome ? consisting of hypertelorism, aortic root dilatation/aneurysm, and cleft palate or bifid uvula ? was present in all 6 cases. Interestingly, none of the 5 individuals who underwent psychological evaluation showed developmental delay. The pattern of all other LDS features showed interindividual variability. Our data support the recently reported observation that symptoms of LDS can develop at a very young age, making early diagnosis and management essential for these patients. This is the first report on a Polish infant with typical LDS symptoms caused by a TGFBR2 mutation.
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