Lisch nodules and iris mammillations in two siblings with familial legius syndrome
Legius syndrome is characterized by numerous café-au-lait macules and intertriginous freckling, but typically lacks the distinctive tumor manifestations of neurofibromatosis type 1. We report two siblings with Legius syndrome and Lisch nodules illustrating the importance of eye surveillance in these...
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Veröffentlicht in: | Clinical case reports 2020, Vol.8 (10), p.1867-1871 |
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creator | Bixel, Kaitlyn D Cano, Miguel J Johnson, Damon M Gomez, Benjamin Lobsinger, Laura V Valentin, Frank E Hsieh, David T Rohena, Luis O |
description | Legius syndrome is characterized by numerous café-au-lait macules and intertriginous freckling, but typically lacks the distinctive tumor manifestations of neurofibromatosis type 1. We report two siblings with Legius syndrome and Lisch nodules illustrating the importance of eye surveillance in these patients. |
doi_str_mv | 10.1002/ccr3.2861 |
format | Report |
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source | DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Online Library Open Access; PubMed Central |
title | Lisch nodules and iris mammillations in two siblings with familial legius syndrome |
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