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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...

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Autores principales: Gutierrez-Castillo, Alejandro, Jimenez-Ruiz, Amado, Chavez-Castillo, Melissa, Ruiz-Sandoval, José Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2018
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.
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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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