Membranoproliferative glomerulonephritis in a child with Prader-Willi syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference6 articles.
1. Prader-Willi syndrome: Current understanding of cause and diagnosis
2. Turner’s Syndrome, 46X, del (X) (p 11), Persistent Complement Activation and Membranoproliferative Glomerulonephritis
3. (1975) Prader-Labhart-Willi syndrome (PLW syndrome). In (ed): “Endocrine and Genetic Disease of Childhood and Adolescence.” Philadelphia: W.B. Saunders Company, pp 1324-1328.
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1. Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review;Frontiers in Endocrinology;2023-07-21
2. Severe Intimal Thickening of Interlobular Arteries Revealed by a Renal Biopsy in an Adult with Prader-Willi Syndrome Complicated by IgA Nephropathy;Internal Medicine;2016
3. P;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007
4. Death in adults with Prader-Willi syndrome may be correlated with maternal uniparental disomy;Journal of Medical Genetics;2003-05-01
5. Membranoproliferative glomerulonephritis type III;Pediatric Nephrology;1998-08-18
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