نتایج جستجو برای: osteodystrophy

تعداد نتایج: 914  

Journal: :Nephrology Dialysis Transplantation 2002

Journal: :Nephrology Dialysis Transplantation 2002

2010
D. Miller

2013 whose GFR is reduced due to intrinsic parenchymal damage as opposed to age-related reductions in GFR without another specific intrinsic renal diagnosis. At each level of CKD there may exist a specific form of renal osteodystrophy. The earliest form of renal bone disease (secondary hyperparathyroidism) may be defined by quantitative histomorphometry and/or biochemical profiling (elevated 1-...

Journal: :Indian journal of pediatrics 2006
Seema Kapoor Siddhartha Gogia Ritu Paul Sharmila Banerjee

Albright's hereditary osteodystrophy is a rare inherited metabolic disorder characterized by a typical phenotype. It may be associated with or without resistance to parathyroid hormone (pseudohypoparathyroidism). Both forms may co-exist in the same family. Pseudohypoparathyroidism Type 1 and Pseudo-pseudohypoparathyroidism occur as a consequence of reduced erythrocyte membrane coupled with Gs a...

2002
Mônica Fernandes Gomes Ana Maria Albernaz Camargo Tatiane Alves Sampaio Maria Aparecida O. C. Graziozi Mônica Costa Armond

Albright hereditary osteodystrophy is a hereditary metabolic disorder of dominant autosomal etiology that is commonly characterized by short stature, round face, small metacarpus and metatarsus, mental retardation, osteoporosis, subcutaneous calcification, variable hypocalcemia, and hyperphosphatemia. In this study, we report a clinical case of a 17-year-old woman with Albright hereditary osteo...

2007
E. CARROLL

The Journal of Lancaster General Hospital • Winter 2006 • Vol. 1 – No. 3 ABSTRACT Chronic kidney disease (CKD) is a complex syndrome with a variety of comorbidities; in patients on hemodialysis, the most common are cardiovascular disease (CVD) and metabolic bone disease (renal osteodystrophy).1 The pathogenesis of renal osteodystrophy involves abnormal vitamin D levels and secondary hyperparath...

Journal: :Indian pediatrics 2011
Meenakshi Girish Nilofer Mujawar Atul Salodkar

DOOR syndrome is a rare multisystem genetic disorder, consisting of deafness (sensorineural), onychodystrophy, osteodystrophy, and mental retardation. Seizures reported frequently in this condition are often refractory to treatment.

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1998
K Hruska

number, and an increase in the number of osteoclastic Introduction resorption bays demonstrating the increased rates of bone resorption in osteitis fibrosa. Renal osteodystrophy is the term used to describe the In addition, osteitis fibrosa is characterized by a skeletal complications of end-stage renal disease. It is prominent accumulation of fibroblastic cells around a multifactorial disorder...

Journal: :World Journal of Gastroenterology 2010

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