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Septo-optic Dysplasia Plus Syndrome
Septo-optic dysplasia plus is a rare congenital syndrome characterized by the classic triad of optic nerve hypoplasia, hypothalamic-hypophyseal dysfunction, and midline abnormalities, with associated malformations of cortical development. Clinical manifestations include optic nerve disease, epilepsy...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384050/ https://www.ncbi.nlm.nih.gov/pubmed/30800538 http://dx.doi.org/10.7759/cureus.3727 |
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author | Gutierrez-Castillo, Alejandro Jimenez-Ruiz, Amado Chavez-Castillo, Melissa Ruiz-Sandoval, José Luis |
author_facet | Gutierrez-Castillo, Alejandro Jimenez-Ruiz, Amado Chavez-Castillo, Melissa Ruiz-Sandoval, José Luis |
author_sort | Gutierrez-Castillo, Alejandro |
collection | PubMed |
description | Septo-optic dysplasia plus is a rare congenital syndrome characterized by the classic triad of optic nerve hypoplasia, hypothalamic-hypophyseal dysfunction, and midline abnormalities, with associated malformations of cortical development. Clinical manifestations include optic nerve disease, epilepsy, intellectual delay, and endocrine dysfunction. We present the case of an 18-year-old man with a history of seizures, growth hormone deficiency, and optic nerve disease that was diagnosed with septo-optic dysplasia plus syndrome with characteristic imaging findings. |
format | Online Article Text |
id | pubmed-6384050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-63840502019-02-23 Septo-optic Dysplasia Plus Syndrome Gutierrez-Castillo, Alejandro Jimenez-Ruiz, Amado Chavez-Castillo, Melissa Ruiz-Sandoval, José Luis Cureus Endocrinology/Diabetes/Metabolism Septo-optic dysplasia plus is a rare congenital syndrome characterized by the classic triad of optic nerve hypoplasia, hypothalamic-hypophyseal dysfunction, and midline abnormalities, with associated malformations of cortical development. Clinical manifestations include optic nerve disease, epilepsy, intellectual delay, and endocrine dysfunction. We present the case of an 18-year-old man with a history of seizures, growth hormone deficiency, and optic nerve disease that was diagnosed with septo-optic dysplasia plus syndrome with characteristic imaging findings. Cureus 2018-12-13 /pmc/articles/PMC6384050/ /pubmed/30800538 http://dx.doi.org/10.7759/cureus.3727 Text en Copyright © 2018, Gutierrez-Castillo et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Endocrinology/Diabetes/Metabolism Gutierrez-Castillo, Alejandro Jimenez-Ruiz, Amado Chavez-Castillo, Melissa Ruiz-Sandoval, José Luis Septo-optic Dysplasia Plus Syndrome |
title | Septo-optic Dysplasia Plus Syndrome |
title_full | Septo-optic Dysplasia Plus Syndrome |
title_fullStr | Septo-optic Dysplasia Plus Syndrome |
title_full_unstemmed | Septo-optic Dysplasia Plus Syndrome |
title_short | Septo-optic Dysplasia Plus Syndrome |
title_sort | septo-optic dysplasia plus syndrome |
topic | Endocrinology/Diabetes/Metabolism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384050/ https://www.ncbi.nlm.nih.gov/pubmed/30800538 http://dx.doi.org/10.7759/cureus.3727 |
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