Evidence map›Paper›PMID 38076278›Full record

ArticleEpilepsy & behavior reports2023

Early onset developmental and epileptic encephalopathy and Rett-like phenotype in a 15-year-old girl affected by Cornelia de Lange syndrome type 2 due to a

L Parmeggiani, F Stanzial, E Menna, E Boni, F Manzoni, F Benedicenti, S Pellegrin

Open access · goldAbstract read
In one paragraph

Article in Epilepsy & behavior reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 22% of its field
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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
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 at 1 institution in 1 country.

L ParmeggianiChild Neurology and Rehabilitation Service - Regional Hospital of Bolzano, Via Lorenz Böhler, 5, 39100 Bolzano (BZ), Italy.
F StanzialGenetic Counseling Service - Regional Hospital of Bolzano, Via Lorenz Böhler, 5, 39100 Bolzano (BZ), Italy.
E MennaChild Neurology and Rehabilitation Service - Regional Hospital of Bolzano, Via Lorenz Böhler, 5, 39100 Bolzano (BZ), Italy.
E BoniChild Neurology and Rehabilitation Service - Regional Hospital of Bolzano, Via Lorenz Böhler, 5, 39100 Bolzano (BZ), Italy.
F ManzoniChild Neurology and Rehabilitation Service - Regional Hospital of Bolzano, Via Lorenz Böhler, 5, 39100 Bolzano (BZ), Italy.
F BenedicentiGenetic Counseling Service - Regional Hospital of Bolzano, Via Lorenz Böhler, 5, 39100 Bolzano (BZ), Italy.
S PellegrinChild Neurology and Rehabilitation Service - Regional Hospital of Bolzano, Via Lorenz Böhler, 5, 39100 Bolzano (BZ), Italy.
Ospedale di Bolzano · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developmental and epileptic encephalopathies (DEE) are conditions in which a mutated gene may cause abnormal functioning of the central nervous system, resulting in both encephalopathy and epileptogenesis. We present a case of a girl with a DEE characterized by a Rett-like phenotype in association with febrile and afebrile clusters of focal seizures. The girl presented typical development until the age of 18 months, followed by regression. The first febrile bilateral tonic-clonic seizure was observed at 30 months of age, and the following month seizures recurred in clusters of several episodes per day every 10 days. These seizures were characterized by behavioural arrest, emotional symptoms, head turning, and followed by bilateral tonic-clonic seizures. The administration of valproic acid and levetiracetam led to prolonged seizure control. However, from the age of 7 years, she had monthly recurrent clusters of focal seizures and non-convulsive status epilepticus which occurred at different ages. Brain and spinal cord MRI showed mild non-progressive hemispheric cerebellar atrophy. A next generation sequencing panel for epilepsy identified the

Indexed as

Developmental and epileptic encephalopathyDevelopmental regressionEpilepsyNeurodevelopmental disorderPCDH19-related epilepsySMC1A

Identifiers

PMID38076278
PMCPMC10709160
OpenAlexW4388673193

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.