Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported
Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of cranio...
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Veröffentlicht in: | Archives of Pediatric Neurosurgery 2024-01, Vol.6 (1), p.e1942023 |
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creator | Koko, Aliyu Muhammad Lasseini, Ali Jinjiri Isma, Nasiru Bala Shehu, Bello |
description | Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele
Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.
Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele
Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome. |
doi_str_mv | 10.46900/apn.v5i3.194 |
format | Article |
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Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.
Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele
Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.</description><identifier>ISSN: 2675-3626</identifier><identifier>EISSN: 2675-3626</identifier><identifier>DOI: 10.46900/apn.v5i3.194</identifier><language>eng</language><publisher>Sociedade Brasileira de Neurocirurgia Pediatrica</publisher><subject>Birth defects ; Conjoined twins ; Genetic disorders ; Hydrocephalus ; Myelomeningocele</subject><ispartof>Archives of Pediatric Neurosurgery, 2024-01, Vol.6 (1), p.e1942023</ispartof><rights>COPYRIGHT 2024 Sociedade Brasileira de Neurocirurgia Pediatrica</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-3742-5075 ; 0000-0002-7166-5734 ; 0009-0003-6601-6048 ; 0000-0001-9032-5172</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Koko, Aliyu Muhammad</creatorcontrib><creatorcontrib>Lasseini, Ali</creatorcontrib><creatorcontrib>Jinjiri Isma, Nasiru</creatorcontrib><creatorcontrib>Bala Shehu, Bello</creatorcontrib><title>Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported</title><title>Archives of Pediatric Neurosurgery</title><description>Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele
Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.
Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele
Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.</description><subject>Birth defects</subject><subject>Conjoined twins</subject><subject>Genetic disorders</subject><subject>Hydrocephalus</subject><subject>Myelomeningocele</subject><issn>2675-3626</issn><issn>2675-3626</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpNkMFOwzAQRC0EElXpkbt_IMF2bCfhVkVAkYpACM7RxlmnRmkS2WlR_p5Ae0B72N3RzBweIbecxVLnjN3B0MVH5ZKY5_KCLIROVZRooS__3ddkFcIXY0xkSmciWRB8Aw_Bjc7QwkPn-gGaQ6DfbtzRAv3RGWjpy4Rtv8fOdU1vsEUKXU03U-3nb9hBewj39B2H3o-zg447pB48ttNZxPqGXFloA67Oe0k-Hx8-ik20fX16LtbbyAguZWSVYZkUNU95hZArrpjVrDKMK1EnORhEXaGowEqroK5krhPOQWXAtEXMkiWJT70NtFi6zvajBzNPjXtn-g6tm_V1mok0k4rlcyA6BYzvQ_Boy8G7Pfip5Kz841rOXMtfruXMNfkB6QNubA</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Koko, Aliyu Muhammad</creator><creator>Lasseini, Ali</creator><creator>Jinjiri Isma, Nasiru</creator><creator>Bala Shehu, Bello</creator><general>Sociedade Brasileira de Neurocirurgia Pediatrica</general><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><orcidid>https://orcid.org/0000-0002-3742-5075</orcidid><orcidid>https://orcid.org/0000-0002-7166-5734</orcidid><orcidid>https://orcid.org/0009-0003-6601-6048</orcidid><orcidid>https://orcid.org/0000-0001-9032-5172</orcidid></search><sort><creationdate>20240101</creationdate><title>Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported</title><author>Koko, Aliyu Muhammad ; Lasseini, Ali ; Jinjiri Isma, Nasiru ; Bala Shehu, Bello</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2144-f5c0842d171bea95150f60bc0152d39acee6be2baf4f5adb496311a58a06fee83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Birth defects</topic><topic>Conjoined twins</topic><topic>Genetic disorders</topic><topic>Hydrocephalus</topic><topic>Myelomeningocele</topic><toplevel>online_resources</toplevel><creatorcontrib>Koko, Aliyu Muhammad</creatorcontrib><creatorcontrib>Lasseini, Ali</creatorcontrib><creatorcontrib>Jinjiri Isma, Nasiru</creatorcontrib><creatorcontrib>Bala Shehu, Bello</creatorcontrib><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><jtitle>Archives of Pediatric Neurosurgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koko, Aliyu Muhammad</au><au>Lasseini, Ali</au><au>Jinjiri Isma, Nasiru</au><au>Bala Shehu, Bello</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported</atitle><jtitle>Archives of Pediatric Neurosurgery</jtitle><date>2024-01-01</date><risdate>2024</risdate><volume>6</volume><issue>1</issue><spage>e1942023</spage><pages>e1942023-</pages><issn>2675-3626</issn><eissn>2675-3626</eissn><abstract>Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele
Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.
Objective: parasitic craniopagus is an extremely rare neurosurgical condition globally, additional anomalies such as hydrocephalus and myelomeningocele make it even more uncommon and complex to manage. The objective of this report was to describe successful management of a child with triad of craniopagus parasiticus, congenital hydrocephalus and cervical myelomeningocele
Case presentation: we successfully managed a five-month-old female infant with parasitic craniopagus, cervical myelomeningocele and congenital hydrocephalus.
Conclusion: parasitic craniopagus remains an uncommon neurosurgical condition and can be associated with many congenital anomalies such as hydrocephalus and myelomeningocele, careful evaluation and management will confer favourable outcome.</abstract><pub>Sociedade Brasileira de Neurocirurgia Pediatrica</pub><doi>10.46900/apn.v5i3.194</doi><orcidid>https://orcid.org/0000-0002-3742-5075</orcidid><orcidid>https://orcid.org/0000-0002-7166-5734</orcidid><orcidid>https://orcid.org/0009-0003-6601-6048</orcidid><orcidid>https://orcid.org/0000-0001-9032-5172</orcidid><oa>free_for_read</oa></addata></record> |
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source | EZB-FREE-00999 freely available EZB journals |
subjects | Birth defects Conjoined twins Genetic disorders Hydrocephalus Myelomeningocele |
title | Parasitic Craniopagus with Cervical Myelomeningocele and Hydrocephalus: Reporting the rarely Reported |
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