File:Rothmund-Thomson syndrome.jpg

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Rothmund-Thomson_syndrome.jpg(628 × 523 pixels, file size: 54 KB, MIME type: image/jpeg)

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English: Panel showing some clinical features of the RTS syndrome. A) Chronic phase of cheek poikiloderma (4-year-old girl). B) Poikiloderma with alopecia (21-year-old boy). C) Poikiloderma. D) Poikiloderma sparing the trunk (courtesy of Professor M. Paradisi, Rome). E) Photo distributed poikiloderma and valgism of the knees. F) Thumb aplasia (patient B). G) Bone defect seen by X-Rays: cystic-like destructive lesion of the humerus (distal epiphysis) without apparent solution of continuity of the cortical bone (patient E).
Date
Source Lidia Larizza, Gaia Roversi, Ludovica Volpi (2010) Rothmund-Thomson syndrome. Orphanet Journal of Rare Diseases 2010, 5:2doi:10.1186/1750-1172-5-2
Author Lidia Larizza, Gaia Roversi, Ludovica Volpi
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current21:54, 13 December 2010Thumbnail for version as of 21:54, 13 December 2010628 × 523 (54 KB)commons>Filip em{{Information |Description={{en|1=Panel showing some clinical features of the RTS syndrome. A) Chronic phase of cheek poikiloderma (4-year-old girl). B) Poikiloderma with alopecia (21-year-old boy). C) Poikiloderma. D) Poikiloderma sparing the trunk (cour

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