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1.
Clin Nephrol ; 71(1): 80-3, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19203555

ABSTRACT

BACKGROUND: Familial juvenile hyperuricemic nephropathy (FJHN) is a rare autosomal dominant disease caused by mutations in the uromodulin gene (UMOD) and leading to gout, tubulointerstitial nephropathy and end-stage renal disease. CASE REPORTS AND RESULTS: A Latvian family suffering from FJHN is described. The father of the family developed ESRD at age 36. His daughter was diagnosed with gout and chronic kidney disease at age 14 years. A renal biopsy revealed tubulointerstitial disease; 2 sons were diagnosed at age 9 and 4 with elevated uric acid levels and reduced fractional uric acid excretion. Urinary uromodulin was normal in the younger boy, but markedly decreased in the 2 other patients. Genetic analysis revealed a previously undescribed D196Y mutation in the UMOD gene. The female patient became pregnant at age 23. During pregnancy serum creatinine decreased from 2.0 to 1.5 mg/dl and blood pressure remained low. Analysis of the baby's umbilical cord blood and a mouth swab showed the presence of the D196Y mutation. Its urinary uromodulin excretion was in the low normal range. CONCLUSION: The uromodulin excretion pattern observed in the investigated family suggests that urinary uromodulin decreases in FJHN from low normal values at childhood to extremely low levels in early adulthood. In addition, this first report on pregnancy in a patient with FJHN shows normal adaptation despite markedly reduced renal function.


Subject(s)
Hyperuricemia/genetics , Kidney Diseases/genetics , Mucoproteins/genetics , Mutation/genetics , Pregnancy Complications/genetics , Adolescent , Age Factors , Child, Preschool , Female , Humans , Hyperuricemia/metabolism , Hyperuricemia/therapy , Infant, Newborn , Kidney Diseases/metabolism , Kidney Diseases/therapy , Male , Mucoproteins/metabolism , Pedigree , Pregnancy , Pregnancy Complications/metabolism , Pregnancy Complications/therapy , Pregnancy Outcome , Uromodulin , Young Adult
2.
J Colloid Interface Sci ; 276(2): 284-9, 2004 Aug 15.
Article in English | MEDLINE | ID: mdl-15271554

ABSTRACT

Standard isotherms of the sorption of water, methanol, and benzene vapors on cellulose using a cellulose standard are determined. The standard, namely, mesoporous cellulose with specific surface of up to 350 m2/g, is obtained by the method of exchanging water in swollen cellulose with organic solvents. A comparison of the experimental sorption isotherm with the standard isotherm makes it possible to determine the specific surface of celluloses accessible a the given sorbate and, in combination with the Brunauer-Emmett-Teller adsorption equation, to characterize their surface properties. The identity of the sorption properties of the initial and dewatered (porous) celluloses relative to active vapors is shown, which evidences the assumed mechanism of swelling as the sorbent's division into morphological structures with the formation of new surface. A comparative analysis of the sorption properties of cellulose and silica, whose nature of active sorption centers is similar (weak acid hydroxyl groups), has been made. The affinity of the standard isotherms and close values of the cross-sectional area of different sorbates on both sorbents testify the similarity in their sorption behavior. Thus, the processes of sorption with rigid and swelling sorbents can be regarded in a unified context. Therefore, the adsorption models developed for rigid sorbents can be applied to cellulose sorbents to analyze their sorption properties.


Subject(s)
Benzene/chemistry , Cellulose/chemistry , Methanol/chemistry , Solvents/chemistry , Water/chemistry , Adsorption , Porosity , Solubility , Volatilization
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