Congenital Bilateral Perisylvian Syndrome Associated with Pierre Robin Sequence: a Case Report
Introduction: Pierre Robin sequence is characterized by the classic triad of congenital micrognathia, glossoptosis, and airway obstruction. It is caused by various etiologies, including cortical development malformations as seen in congenital perisylvian syndrome. Clinical Case Presentation: We rep...
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| Format: | Article |
| Language: | Spanish |
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Universidad de Antioquia
2025-01-01
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| Series: | Iatreia |
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| Online Access: | https://revistas.udea.edu.co/index.php/iatreia/article/view/350773 |
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| author | Castro-Murillo, Julio Cesar Gómez-Guzmán, Enid Leticia Rojas-Cerón, Christian Andrés |
| author_facet | Castro-Murillo, Julio Cesar Gómez-Guzmán, Enid Leticia Rojas-Cerón, Christian Andrés |
| author_sort | Castro-Murillo, Julio Cesar |
| collection | DOAJ |
| description | Introduction: Pierre Robin sequence is characterized by the classic triad of congenital micrognathia, glossoptosis, and airway obstruction. It is caused by various etiologies, including cortical development malformations as seen in congenital perisylvian syndrome.
Clinical Case Presentation: We report a case of a 31-week preterm newborn girl who exhibited the classic triad of Pierre Robin sequence during physical examination, later developing complications such as epileptic seizures, airway obstruction, and swallowing disorder. During the etiological investigation, cerebral magnetic resonance imaging revealed bilateral polymicrogyria, confirming a diagnosis of bilateral perisylvian syndrome.
Conclusions: Cortical development malformations, such as congenital bilateral perisylvian syndrome, are part of the etiological spectrum in Pierre Robin sequence, especially those presenting with pseudobulbar paralysis, epileptic seizures, and central origin hypotonia. |
| format | Article |
| id | doaj-art-d5817cb414c74b9c83eb252f7da25ad9 |
| institution | Kabale University |
| issn | 0121-0793 2011-7965 |
| language | Spanish |
| publishDate | 2025-01-01 |
| publisher | Universidad de Antioquia |
| record_format | Article |
| series | Iatreia |
| spelling | doaj-art-d5817cb414c74b9c83eb252f7da25ad92025-01-17T15:50:06ZspaUniversidad de AntioquiaIatreia0121-07932011-79652025-01-0138115816410.17533/udea.iatreia.279Congenital Bilateral Perisylvian Syndrome Associated with Pierre Robin Sequence: a Case ReportCastro-Murillo, Julio Cesar 0https://orcid.org/0000-0001-6535-1248Gómez-Guzmán, Enid Leticia1https://orcid.org/0000-0002-4957-6591Rojas-Cerón, Christian Andrés2https://orcid.org/0000-0001-9690-5485Universidad del Valle, Cali, ColombiaUniversidad del Valle, Cali, ColombiaUniversidad del Valle, Cali, ColombiaIntroduction: Pierre Robin sequence is characterized by the classic triad of congenital micrognathia, glossoptosis, and airway obstruction. It is caused by various etiologies, including cortical development malformations as seen in congenital perisylvian syndrome. Clinical Case Presentation: We report a case of a 31-week preterm newborn girl who exhibited the classic triad of Pierre Robin sequence during physical examination, later developing complications such as epileptic seizures, airway obstruction, and swallowing disorder. During the etiological investigation, cerebral magnetic resonance imaging revealed bilateral polymicrogyria, confirming a diagnosis of bilateral perisylvian syndrome. Conclusions: Cortical development malformations, such as congenital bilateral perisylvian syndrome, are part of the etiological spectrum in Pierre Robin sequence, especially those presenting with pseudobulbar paralysis, epileptic seizures, and central origin hypotonia.https://revistas.udea.edu.co/index.php/iatreia/article/view/350773infant prematuremalformations of cortical developmentpierre robin syndromepseudobulbar palsy |
| spellingShingle | Castro-Murillo, Julio Cesar Gómez-Guzmán, Enid Leticia Rojas-Cerón, Christian Andrés Congenital Bilateral Perisylvian Syndrome Associated with Pierre Robin Sequence: a Case Report Iatreia infant premature malformations of cortical development pierre robin syndrome pseudobulbar palsy |
| title | Congenital Bilateral Perisylvian Syndrome Associated with Pierre Robin Sequence: a Case Report |
| title_full | Congenital Bilateral Perisylvian Syndrome Associated with Pierre Robin Sequence: a Case Report |
| title_fullStr | Congenital Bilateral Perisylvian Syndrome Associated with Pierre Robin Sequence: a Case Report |
| title_full_unstemmed | Congenital Bilateral Perisylvian Syndrome Associated with Pierre Robin Sequence: a Case Report |
| title_short | Congenital Bilateral Perisylvian Syndrome Associated with Pierre Robin Sequence: a Case Report |
| title_sort | congenital bilateral perisylvian syndrome associated with pierre robin sequence a case report |
| topic | infant premature malformations of cortical development pierre robin syndrome pseudobulbar palsy |
| url | https://revistas.udea.edu.co/index.php/iatreia/article/view/350773 |
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