Volume 79, Issue 6, Pages (March 2011)

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Volume 79, Issue 6, Pages 691-692 (March 2011) The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy Claudia Izzi, Pietro Maffei, Gabriella Milan, Regina Tardanico, Paolo Foini, Jan Marshall, Alessandra Marega, Francesco Scolari Kidney International Volume 79, Issue 6, Pages 691-692 (March 2011) DOI: 10.1038/ki.2010.514 Copyright © 2011 International Society of Nephrology Terms and Conditions

Figure 1 Endomyocardial biopsy showing severe interstitial fibrosis and moderate myocellular hypertrophy (hematoxylin and eosin; original magnification×20). Kidney International 2011 79, 691-692DOI: (10.1038/ki.2010.514) Copyright © 2011 International Society of Nephrology Terms and Conditions

Figure 2 Renal biopsy showing focal areas of interstitial fibrosis and tubular atrophy and normal glomeruli (hematoxylin and eosin; original magnification×100). Kidney International 2011 79, 691-692DOI: (10.1038/ki.2010.514) Copyright © 2011 International Society of Nephrology Terms and Conditions

Figure 3 Haplotype of kindred surrounding the ALMS1 region. Arrow indicates the index case. Males and females are indicated by squares and circles, respectively; blackened circles and squares represent affected individuals; gray shading indicates a possible case of Alström syndrome with infantile congestive heart failure, but no other genetic or clinical information is available. Slash indicates deceased individuals from whom DNA was not available. Both affected individuals share a common haplotype defined by markers 16770, D2S210, D2S1394, D2S2111, D2S2109, and D2S286. Kidney International 2011 79, 691-692DOI: (10.1038/ki.2010.514) Copyright © 2011 International Society of Nephrology Terms and Conditions