Evidence map›Paper›PMID 39359952›Full record

ArticleMolecular syndromology2024

Atlantoaxial Instability due to Os Odontoideum in a Child with Christianson Syndrome.

Nezaket Ezgi Güven, Hacer Uçmak, Çiğdem İlter Uçar, Merve Havan, Miraç Yıldırım, Serap Teber, Tanıl Kendirli

Abstract read
In one paragraph

Article in Molecular syndromology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Nezaket Ezgi GüvenDepartment of Pediatrics, Ankara University Faculty of Medicine, Ankara, Turkey.
Hacer UçmakDivision of Pediatric Intensive Care, Department of Pediatrics, Ankara University Faculty of Medicine, Ankara, Turkey.
Çiğdem İlter UçarDivision of Pediatric Neurology, Department of Pediatrics, Ankara University Faculty of Medicine, Ankara, Turkey.
Merve HavanDivision of Pediatric Intensive Care, Department of Pediatrics, Ankara University Faculty of Medicine, Ankara, Turkey.
Miraç YıldırımDivision of Pediatric Neurology, Department of Pediatrics, Ankara University Faculty of Medicine, Ankara, Turkey.
Serap TeberDivision of Pediatric Neurology, Department of Pediatrics, Ankara University Faculty of Medicine, Ankara, Turkey.
Tanıl KendirliDivision of Pediatric Intensive Care, Department of Pediatrics, Ankara University Faculty of Medicine, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Christianson syndrome is a rare neurodevelopmental disorder associated with mutations in the Case Presentation: A 5-year-old boy was presented with respiratory failure and then progressive muscle weakness in all four extremities. He manifested acquired microcephaly, intellectual disability, global developmental delay, distinct dysmorphic facial features, seizures, spastic tetraparesis, truncal hypotonia, speech impairment, failure to thrive, malnutrition, recurrent lung infections, self-mutilation, primary hyperparathyroidism, medullary nephrocalcinosis, and atlantoaxial instability due to os odontoideum. Brain magnetic resonance imaging revealed atlantoaxial instability due to os odontoideum, a narrow foramen magnum, myelopathy due to spinal cord compression, and cerebral and cerebellar atrophy. Discussion: This report highlights a significant contribution by introducing a child with Christianson syndrome describing atlantoaxial instability due to os odontoideum, a previously undocumented phenomenon. This report suggests a potential link between Christianson syndrome and atlantoaxial instability. In children with Christianson syndrome experiencing increased muscle weakness in all extremities during follow-up, consideration of underlying myelopathy due to os odontoideum is advised.

Indexed as

Atlantoaxial instabilityChristianson syndromeMedullary nephrocalcinosisOs odontoideumPrimary hyperparathyroidismSLC9A6

Identifiers

PMID39359952
PMCPMC11444701

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.