Evidence map›Paper›PMID 36321570›Full record

ArticleAmerican journal of medical genetics. Part A2023

Further characterization of NFIB-associated phenotypes: Report of two new individuals.

Gemma Marinella, Eugenia Conti, Bianca Buchignani, Giada Sgherri, Rosa Pasquariello, Flavio Giordano, Paola Cristofani, Roberta Battini, Agatino Battaglia

Open access · hybridAbstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part A, 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
1.3field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  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

9 authors at 3 institutions in 1 country.

Gemma MarinellaDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, Calambrone, Pisa, Italy.
Eugenia ContiDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, Calambrone, Pisa, Italy.
Bianca BuchignaniDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, Calambrone, Pisa, Italy.
Giada SgherriDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, Calambrone, Pisa, Italy.
Rosa PasquarielloDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, Calambrone, Pisa, Italy.
Flavio GiordanoDepartment of Neurosurgery, Children's Hospital A. Meyer-University of Florence, Firenze, Florence, Italy.
Paola CristofaniDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, Calambrone, Pisa, Italy.
Roberta BattiniDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, Calambrone, Pisa, Italy.ORCID 0000-0002-7889-1355
Agatino BattagliaDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, Calambrone, Pisa, Italy.ORCID 0000-0002-7128-7606
Fondazione Stella Maris · ITUniversity of Pisa · ITMeyer Children's Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear Factor I B (NFIB) haploinsufficiency has recently been identified as a cause of intellectual disability (ID) and macrocephaly. Here we report on two new individuals carrying a microdeletion in the chromosomal region 9p23-p22.3 containing NFIB. The first is a 7-year 9-month old boy with developmental delays, ID, definite facial anomalies, and brain and spinal cord magnetic resonance imaging findings including periventricular nodular heterotopia, hypoplasia of the corpus callosum, arachnoid cyst in the left middle cranial fossa, syringomyelia in the thoracic spinal cord and distal tract of the conus medullaris, and a stretched appearance of the filum terminale. The second is a 32-year-old lady (the proband' mother) with dysmorphic features, and a history of learning disability, hypothyroidism, poor growth, left inguinal hernia, and panic attacks. Her brain magnetic resonance imaging findings include a dysmorphic corpus callosum, and a small cyst in the left choroidal fissure that marks the hippocampal head. Array-based comparative genomic hybridization identified, in both, a 232 Kb interstitial deletion at 9p23p22.3 including several exons of NFIB and no other known genes. Our two individuals add to the knowledge of this rare disorder through the addition of new brain and spinal cord MRI findings and dysmorphic features. We propose that NFIB haploinsufficiency causes a clinically recognizable malformation-ID syndrome.

Indexed as

Abnormalities, MultipleIntellectual DisabilityAdultBrainChildChromosome DeletionComparative Genomic HybridizationCorpus CallosumFemaleHumansMaleNFI Transcription FactorsPhenotypeNFIB protein, humanNFI Transcription Factorsbrain/spinal cord malformationdevelopmental delayintellectual disabilityNFIBperiventricular nodular heterotopiasyringomyelia

Identifiers

PMID36321570
PMCPMC10091694
OpenAlexW4307975131

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.