Results 121 to 130 of about 2,138 (167)
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Pediatric Radiology, 1982
Skeletal survey in an 8-year-old girl with primary hyperoxaluria and in chronic renal failure revealed wide translucent metaphyseal bands and defects at the ends of the long bones. Similar disordered bone growth was seen as rims of rarefaction around the large epiphyses, the patella and the tarsal bones. Bone density was generally increased.
J, Wiggelinkhuizen, R M, Fisher
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Skeletal survey in an 8-year-old girl with primary hyperoxaluria and in chronic renal failure revealed wide translucent metaphyseal bands and defects at the ends of the long bones. Similar disordered bone growth was seen as rims of rarefaction around the large epiphyses, the patella and the tarsal bones. Bone density was generally increased.
J, Wiggelinkhuizen, R M, Fisher
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American Journal of Obstetrics and Gynecology, 1962
0 x A L o s I s is a rare disease characterized by hyperoxaluria and widespread deposits of oxalate crystals throughout the body.‘-’ DoIan* has recently reviewed oxalosis and was unable to find a proved case in pregnancy or the puerperium. His review includes some 39 cases and ascribes the initial description of the disease entity to Lepoutre,” in 1925.
R J, HILDEBRANDT, D R, SHANKLIN
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0 x A L o s I s is a rare disease characterized by hyperoxaluria and widespread deposits of oxalate crystals throughout the body.‘-’ DoIan* has recently reviewed oxalosis and was unable to find a proved case in pregnancy or the puerperium. His review includes some 39 cases and ascribes the initial description of the disease entity to Lepoutre,” in 1925.
R J, HILDEBRANDT, D R, SHANKLIN
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Pediatrics, 1952
A case is reported of renal failure in a boy subsequent to recurrent calcium oxalate urinary calculi. The post mortem disclosed widespread deposits in the tissues of calcium oxalate crystals. These were particularly prominent in the kidneys and bone marrow. It is suggested that this is the end result of an "inborn error of metabolism" in
L. YING CHOU, W. L. DONOHUE
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A case is reported of renal failure in a boy subsequent to recurrent calcium oxalate urinary calculi. The post mortem disclosed widespread deposits in the tissues of calcium oxalate crystals. These were particularly prominent in the kidneys and bone marrow. It is suggested that this is the end result of an "inborn error of metabolism" in
L. YING CHOU, W. L. DONOHUE
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Archives of Ophthalmology, 1989
A 55-year-old woman with chronic renal failure treated with hemodialysis had severe bilateral visual loss develop due to retinal ischemia. Ophthalmoscopy showed crystals in the distribution of the retinal arteries, but not veins, and this led to a diagnosis of systemic oxalosis.
C G, Wells +4 more
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A 55-year-old woman with chronic renal failure treated with hemodialysis had severe bilateral visual loss develop due to retinal ischemia. Ophthalmoscopy showed crystals in the distribution of the retinal arteries, but not veins, and this led to a diagnosis of systemic oxalosis.
C G, Wells +4 more
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Blood, 2012
![Figure][1] A 28-year-old woman presented with pancytopenia. Her past medical history was significant for primary hyperoxaluria. She had recurrent renal stones and urinary tract infections since the age of 5 years.
Nasir A, Bakshi, Hazzaa, Al-Zahrani
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![Figure][1] A 28-year-old woman presented with pancytopenia. Her past medical history was significant for primary hyperoxaluria. She had recurrent renal stones and urinary tract infections since the age of 5 years.
Nasir A, Bakshi, Hazzaa, Al-Zahrani
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Clinical Nuclear Medicine, 1993
Several physiologic and pathologic conditions demonstrating extraosseous localization of bone scanning agents have been described, including metastatic calcification of the soft tissues secondary to metabolic disorders, malignancies, and chronic renal failure.
S, Murthy +4 more
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Several physiologic and pathologic conditions demonstrating extraosseous localization of bone scanning agents have been described, including metastatic calcification of the soft tissues secondary to metabolic disorders, malignancies, and chronic renal failure.
S, Murthy +4 more
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Hand manifestations of oxalosis
The Journal of Hand Surgery, 1993Oxalosis is an unusual metabolic disease that results either from an inherited hepatic enzyme deficiency or as the result of poor oxalate clearance during chronic hemodialysis. We present two cases of oxalosis and describe the hand manifestations of this condition and their treatment.
A A, Freiberg, D N, Fish, D S, Louis
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Autopsy Findings of a Case with Oxalosis
Pediatric and Developmental Pathology, 2006Oxalosis, deposition of calcium oxalate in tissues, is the final stage of hyperoxaluric syndromes. Being a rare entity, it is often missed, or the diagnosis is delayed, since the definitive diagnosis requires special laboratory tests. Kidneys, the walls of blood vessels, and bones are the major sites for crystal deposition.
Doganavsargil, Basak +4 more
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