Evidence map›Paper›PMID 37469362›Full record

ArticleClinical case reports2023

New presentation of CLIFAHDD syndrome with a novel variant in

Bita Hashemi, Richard J Huntsman, Huan Li, Dapeng Zhang, Yanwei Xi

Abstract readCase Reports
In one paragraph

Article in Clinical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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

5 authors.

Bita HashemiDepartment of Pediatrics, Division of Medical Genetics University of Saskatchewan Saskatoon Saskatchewan Canada.ORCID https://orcid.org/0000-0002-5772-008X
Richard J HuntsmanDepartment of Pediatrics, Division of Neurology University of Saskatchewan Saskatoon Saskatchewan Canada.
Huan LiDepartment of Biology, College of Arts and Sciences Saint Louis University Saint Louis Missouri USA.
Dapeng ZhangDepartment of Biology, College of Arts and Sciences Saint Louis University Saint Louis Missouri USA.
Yanwei XiDepartment of Pathology and Laboratory Medicine, Genomics Laboratory University of Saskatchewan Saskatoon Saskatchewan Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Key Clinical Message: Congenital Contractures of Limbs and Face, Hypotonia, and Developmental Delay (CLIFAHDD) syndrome is a recently described type of distal arthrogryposis which unlike other subtypes is associated with developmental delay and various neurologic presentation. Epilepsy and ataxia have been reported. We add paroxysmal dyskinesia to the clinical spectrum. Understanding the molecular mechanism can help developing targeted therapy in future. Abstract: This study resulted in identification of a novel variant in

Indexed as

CLIFAHDD syndromedistal arthrogryposisNALCN gene

Identifiers

PMID37469362
PMCPMC10352546

What OpenQuestion holds

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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.