Evidence map›Paper›PMID 38052889›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2024

Prenatal dispositions and genetic analysis of monozygotic female twins with suprasellar cysts and hydrocephalus: A case report.

Frederikke Guldberg, Carl Christian Larsen, Elsebet Østergaard, Jonathan Carlsen, Marianne Juhler, Tina Nørgaard Munch

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In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Frederikke GuldbergDepartment of Neurosurgery, Copenhagen University Hospital, Copenhagen, Denmark. Frederikke.Guldberg@regionh.dk.ORCID 0009-0009-9647-2566
Carl Christian LarsenDepartment of Neurosurgery, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0009-0000-9554-0031
Elsebet ØstergaardDepartment of Clinical Genetics, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0000-0002-8047-063X
Jonathan CarlsenDepartment of Radiology, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0000-0002-6724-7281
Marianne JuhlerDepartment of Neurosurgery, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0000-0003-2652-7495
Tina Nørgaard MunchDepartment of Neurosurgery, Copenhagen University Hospital, Copenhagen, Denmark.ORCID 0000-0001-5938-000X
Copenhagen University Hospital · DKUniversity of Copenhagen · DKFrederiksberg Hospital · DKStatens Serum Institut · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe present a unique case of monozygotic female twins with virtually identical clinical and radiological presentations of supratentorial hydrocephalus and cystic formations from the suprasellar cistern. DISCUSSION: Evaluating genetic predispositions and prenatal exposures is crucial for hydrocephalus in twins. Familial cases imply a genetic contribution to the development of these anomalies, including chromosomal abnormalities and specific variants linked to arachnoid cyst formation in various syndromes. Extensive genetic analyses found no pathogenic variants in the twins. Prenatal exposure to anti-epileptic medication was known during pregnancy and may be associated with fetal abnormalities, but not central nervous system (CNS) malformations, and was therefore not considered the cause of the condition in the twins. The twins presenting simultaneously with hydrocephalus caused by suprasellar cysts (SAC) underwent a two-step surgical management: initial ventriculoperitoneal shunt (VPS) placement followed by fenestration. Postoperative imaging showed cyst reduction, but a secondary VPS was necessary in both cases.

conclusionGenetic analysis is less likely to identify a monogenic etiology in non-syndromic cases of SACs, which are assumed to be multifactorial. There is no established evidence linking a teratogenic effect of anti-epileptic drugs to CNS malformations. Moreover, the surgical treatment of this complex condition constitutes a point of discussion.

Indexed as

Arachnoid CystsHydrocephalusAnticonvulsantsFemaleGenetic Predisposition to DiseaseHumansPostoperative PeriodPregnancyAnticonvulsantsEndoscopic fenestrationObstructive hydrocephalusPrenatal dispositionsSuprasellar cystTwins

Identifiers

PMID38052889
PMCPMC10891213
OpenAlexW4389396197

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.