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Hao-Fountain syndrome and genital disorders: report of a new possible association

BACKGROUND: Hao-Fountain syndrome is a neurodevelopmental disorder characterized by global developmental delay, variably impaired intellectual development with significant speech delay and, in some males patients, it has been reported an association with hypogonadism. At present less than 50 cases a...

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Autores principales: Zampieri, Nicola, Pulvirenti, Rebecca, Pedrazzoli, Eleonora, Camoglio, Francesco Saverio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9588229/
https://www.ncbi.nlm.nih.gov/pubmed/36273155
http://dx.doi.org/10.1186/s13052-022-01367-7
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author Zampieri, Nicola
Pulvirenti, Rebecca
Pedrazzoli, Eleonora
Camoglio, Francesco Saverio
author_facet Zampieri, Nicola
Pulvirenti, Rebecca
Pedrazzoli, Eleonora
Camoglio, Francesco Saverio
author_sort Zampieri, Nicola
collection PubMed
description BACKGROUND: Hao-Fountain syndrome is a neurodevelopmental disorder characterized by global developmental delay, variably impaired intellectual development with significant speech delay and, in some males patients, it has been reported an association with hypogonadism. At present less than 50 cases are reported in literature. CASE PRESENTATION: We report a case of this rare syndrome in a young female with isolated tubal torsion; our patients had different hospitalizations without treatment but during the last episode we decide to perform an abdominal surgical explortion. This is the first case in Literature with a new USP7 mutation. CONCLUSIONS: This case opens new perspective in this rare syndrome and a review approach to isolated tubal torsion. These symptoms should be always well checked.
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spelling pubmed-95882292022-10-24 Hao-Fountain syndrome and genital disorders: report of a new possible association Zampieri, Nicola Pulvirenti, Rebecca Pedrazzoli, Eleonora Camoglio, Francesco Saverio Ital J Pediatr Case Report BACKGROUND: Hao-Fountain syndrome is a neurodevelopmental disorder characterized by global developmental delay, variably impaired intellectual development with significant speech delay and, in some males patients, it has been reported an association with hypogonadism. At present less than 50 cases are reported in literature. CASE PRESENTATION: We report a case of this rare syndrome in a young female with isolated tubal torsion; our patients had different hospitalizations without treatment but during the last episode we decide to perform an abdominal surgical explortion. This is the first case in Literature with a new USP7 mutation. CONCLUSIONS: This case opens new perspective in this rare syndrome and a review approach to isolated tubal torsion. These symptoms should be always well checked. BioMed Central 2022-10-22 /pmc/articles/PMC9588229/ /pubmed/36273155 http://dx.doi.org/10.1186/s13052-022-01367-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Zampieri, Nicola
Pulvirenti, Rebecca
Pedrazzoli, Eleonora
Camoglio, Francesco Saverio
Hao-Fountain syndrome and genital disorders: report of a new possible association
title Hao-Fountain syndrome and genital disorders: report of a new possible association
title_full Hao-Fountain syndrome and genital disorders: report of a new possible association
title_fullStr Hao-Fountain syndrome and genital disorders: report of a new possible association
title_full_unstemmed Hao-Fountain syndrome and genital disorders: report of a new possible association
title_short Hao-Fountain syndrome and genital disorders: report of a new possible association
title_sort hao-fountain syndrome and genital disorders: report of a new possible association
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9588229/
https://www.ncbi.nlm.nih.gov/pubmed/36273155
http://dx.doi.org/10.1186/s13052-022-01367-7
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