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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Autores principales: Bixel, Kaitlyn D., Cano, Miguel J., Johnson, Damon M., Gomez, Benjamin, Lobsinger, Laura V., Valentin, Frank E., Hsieh, David T., Rohena, Luis O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562883/
https://www.ncbi.nlm.nih.gov/pubmed/33088508
http://dx.doi.org/10.1002/ccr3.2861
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author Bixel, Kaitlyn D.
Cano, Miguel J.
Johnson, Damon M.
Gomez, Benjamin
Lobsinger, Laura V.
Valentin, Frank E.
Hsieh, David T.
Rohena, Luis O.
author_facet Bixel, Kaitlyn D.
Cano, Miguel J.
Johnson, Damon M.
Gomez, Benjamin
Lobsinger, Laura V.
Valentin, Frank E.
Hsieh, David T.
Rohena, Luis O.
author_sort Bixel, Kaitlyn D.
collection PubMed
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.
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spelling pubmed-75628832020-10-20 Lisch nodules and iris mammillations in two siblings with familial legius syndrome Bixel, Kaitlyn D. Cano, Miguel J. Johnson, Damon M. Gomez, Benjamin Lobsinger, Laura V. Valentin, Frank E. Hsieh, David T. Rohena, Luis O. Clin Case Rep Case Reports 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. John Wiley and Sons Inc. 2020-09-01 /pmc/articles/PMC7562883/ /pubmed/33088508 http://dx.doi.org/10.1002/ccr3.2861 Text en Published 2020. This article is a U.S. Government work and is in the public domain in the USA. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Bixel, Kaitlyn D.
Cano, Miguel J.
Johnson, Damon M.
Gomez, Benjamin
Lobsinger, Laura V.
Valentin, Frank E.
Hsieh, David T.
Rohena, Luis O.
Lisch nodules and iris mammillations in two siblings with familial legius syndrome
title Lisch nodules and iris mammillations in two siblings with familial legius syndrome
title_full Lisch nodules and iris mammillations in two siblings with familial legius syndrome
title_fullStr Lisch nodules and iris mammillations in two siblings with familial legius syndrome
title_full_unstemmed Lisch nodules and iris mammillations in two siblings with familial legius syndrome
title_short Lisch nodules and iris mammillations in two siblings with familial legius syndrome
title_sort lisch nodules and iris mammillations in two siblings with familial legius syndrome
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562883/
https://www.ncbi.nlm.nih.gov/pubmed/33088508
http://dx.doi.org/10.1002/ccr3.2861
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