Literature DB >> 19308578

Skeletal features of primary hyperoxaluria type 1, revisited.

Samer El Hage1, Ismat Ghanem, André Baradhi, Chebel Mourani, Samir Mallat, Fernand Dagher, Khalil Kharrat.   

Abstract

PURPOSE: The purpose of this study was to describe the skeletal manifestations of primary hyperoxaluria type 1 (PH1), the most common of the primary hyperoxalurias.
METHODS: We clinically and radiographically reviewed 12 consecutive patients diagnosed with PH1, aged between 2 and 17 years. All patients had evidence of some type of renal involvement, 4 of whom were at end-stage renal disease (ESRD) and were under dialysis.
RESULTS: The main symptom was skeletal pain and was present only in the 4 severely involved patients and appeared during the second year of dialysis. The 2 most severely involved patients had evidence of pathological fractures. Radiological signs were present in patients with or without symptoms. These radiological signs were of two distinct types: those almost specific of oxalosis, such as dense and radiolucent metaphyseal bands and vertebral osteocondensations, which are found mainly in the severely involved individuals, and those less specific, such as signs of renal osteodystrophy, which are also found in less severely involved patients. Interestingly, our study revealed the presence of spondylolysis in 25% of cases. This latter finding is unique and has not previously been reported in the literature.
CONCLUSIONS: The skeletal manifestations of PH1 include specific and less specific radiological signs, with some patients being asymptomatic, and others presenting with bone pain and pathological fractures, as well as spondylolysis.

Entities:  

Year:  2008        PMID: 19308578      PMCID: PMC2656805          DOI: 10.1007/s11832-008-0082-4

Source DB:  PubMed          Journal:  J Child Orthop        ISSN: 1863-2521            Impact factor:   1.548


  32 in total

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Review 2.  The molecular basis of alanine: glyoxylate aminotransferase mistargeting: the most common single cause of primary hyperoxaluria type 1.

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  6 in total

Review 1.  Bone impairment in primary hyperoxaluria: a review.

Authors:  Justine Bacchetta; Georges Boivin; Pierre Cochat
Journal:  Pediatr Nephrol       Date:  2015-01-29       Impact factor: 3.714

Review 2.  Primary hyperoxaluria: spectrum of clinical and imaging findings.

Authors:  Sara B Strauss; Temima Waltuch; William Bivin; Frederick Kaskel; Terry L Levin
Journal:  Pediatr Radiol       Date:  2016-11-14

Review 3.  Update on oxalate crystal disease.

Authors:  Elizabeth C Lorenz; Clement J Michet; Dawn S Milliner; John C Lieske
Journal:  Curr Rheumatol Rep       Date:  2013-07       Impact factor: 4.592

4.  [Late diagnosis of a primary hyperoxaluria in terminal stage of chronic renal failure with severe hypoparathyroidism].

Authors:  Zineb El Ghali; Zineb Ait Lahcen; Wafaa Fadili; Abderrahim Idrissi Kaitouni; Mohamed Hakkou; Abderrachid Hamdaoui; Inass Laouad
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5.  Primary hyperoxaluria detected by bone marrow biopsy: case report.

Authors:  F Nachite; M Dref; A Fakhri; H Rais
Journal:  BMC Clin Pathol       Date:  2017-09-20

Review 6.  Treatment of nongout joint deposition diseases: an update.

Authors:  Tristan Pascart; Pascal Richette; René-Marc Flipo
Journal:  Arthritis       Date:  2014-05-08
  6 in total

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