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Joubert-Plus syndrome with an atretic cephalocele: a case report

Joubert syndrome is a rare heterogeneous disease affecting the cerebellum. It usually presents with hypotonia, abnormal breathing pattern, with distinctive cerebellar and brain stem malformation called the molar tooth sign. It may present with different organ involvement or with other neurological a...

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Autores principales: Al-Smair, Ali, Younes, Sara, Saadeh, Ahmad, Kaoukji, Abdel Rahman, Jaber, Osama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343393/
https://www.ncbi.nlm.nih.gov/pubmed/35928591
http://dx.doi.org/10.1016/j.radcr.2022.07.038
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author Al-Smair, Ali
Younes, Sara
Saadeh, Ahmad
Kaoukji, Abdel Rahman
Jaber, Osama
author_facet Al-Smair, Ali
Younes, Sara
Saadeh, Ahmad
Kaoukji, Abdel Rahman
Jaber, Osama
author_sort Al-Smair, Ali
collection PubMed
description Joubert syndrome is a rare heterogeneous disease affecting the cerebellum. It usually presents with hypotonia, abnormal breathing pattern, with distinctive cerebellar and brain stem malformation called the molar tooth sign. It may present with different organ involvement or with other neurological alterations such as Dandy-Walker syndrome. Joubert syndrome with dandy walker syndrome is called Joubert-Plus syndrome, an exceedingly rare entity. Dandy-Walker syndrome is defined by hypoplasia and upward rotation of the cerebellar vermis and cystic dilation of the fourth ventricle. Atretic cephalocele is another rare diagnosis which is characterized by a herniation of intracranial contents through a skull defect. Herein, we present a case of a 6-month-old patient who presented with floppiness and a scalp nodule. After further evaluation, he was diagnosed with Joubert-Plus syndrome with an atretic cephalocele.
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spelling pubmed-93433932022-08-03 Joubert-Plus syndrome with an atretic cephalocele: a case report Al-Smair, Ali Younes, Sara Saadeh, Ahmad Kaoukji, Abdel Rahman Jaber, Osama Radiol Case Rep Case Report Joubert syndrome is a rare heterogeneous disease affecting the cerebellum. It usually presents with hypotonia, abnormal breathing pattern, with distinctive cerebellar and brain stem malformation called the molar tooth sign. It may present with different organ involvement or with other neurological alterations such as Dandy-Walker syndrome. Joubert syndrome with dandy walker syndrome is called Joubert-Plus syndrome, an exceedingly rare entity. Dandy-Walker syndrome is defined by hypoplasia and upward rotation of the cerebellar vermis and cystic dilation of the fourth ventricle. Atretic cephalocele is another rare diagnosis which is characterized by a herniation of intracranial contents through a skull defect. Herein, we present a case of a 6-month-old patient who presented with floppiness and a scalp nodule. After further evaluation, he was diagnosed with Joubert-Plus syndrome with an atretic cephalocele. Elsevier 2022-07-30 /pmc/articles/PMC9343393/ /pubmed/35928591 http://dx.doi.org/10.1016/j.radcr.2022.07.038 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Al-Smair, Ali
Younes, Sara
Saadeh, Ahmad
Kaoukji, Abdel Rahman
Jaber, Osama
Joubert-Plus syndrome with an atretic cephalocele: a case report
title Joubert-Plus syndrome with an atretic cephalocele: a case report
title_full Joubert-Plus syndrome with an atretic cephalocele: a case report
title_fullStr Joubert-Plus syndrome with an atretic cephalocele: a case report
title_full_unstemmed Joubert-Plus syndrome with an atretic cephalocele: a case report
title_short Joubert-Plus syndrome with an atretic cephalocele: a case report
title_sort joubert-plus syndrome with an atretic cephalocele: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343393/
https://www.ncbi.nlm.nih.gov/pubmed/35928591
http://dx.doi.org/10.1016/j.radcr.2022.07.038
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