Evidence map›Paper›PMID 38348595›Full record

ArticleAmerican journal of medical genetics. Part A2024

EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorder.

Irman Forghani, Steven H Lang, Matthew J Rodier, Stephanie A Bivona, Undiagnosed Diseases Network, Alejo A Morales, Stephan Zuchner, Guney Bademci, Mustafa Tekin

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part A, 2024. 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
3.3field-weighted citation impact, top 9% 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, 6 citations in OpenAlex.

  1. Article
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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 1 institution in 1 country.

Irman ForghaniDepartment of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.ORCID 0000-0002-5484-5186
Steven H LangDepartment of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Matthew J RodierDepartment of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Stephanie A BivonaDepartment of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Undiagnosed Diseases Network
Alejo A MoralesDepartment of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Stephan ZuchnerDepartment of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Guney BademciDepartment of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.ORCID 0000-0002-4052-8833
Mustafa TekinDepartment of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.ORCID 0000-0002-3525-7960
University of Miami · US

Funding

The Undiagnosed Diseases Network Clinical Site of MiamiU01NS134353 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MUSTAFA TEKIN, Stephan Zuchner · 2023 to 2026
$3.1M
Exploring minorities The Undiagnosed Diseases Network Clinical Site of MiamiU01HG010230 · NHGRI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TEKIN, MUSTAFA, ZUCHNER, STEPHAN · 2018 to 2021
$2.6M
UCLA clinical site for the investigation of undiagnosed disordersU01NS134356 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MARTINEZ-AGOSTO, JULIAN, NELSON, STANLEY F. · 2023 to 2023
$936k
NHGRI NIH HHS U01 HG010230NINDS NIH HHS U01 NS134353NINDS NIH HHS U01 NS134356
6 · The paper itself

Abstract

Phenotypic features of a hereditary connective tissue disorder, including craniofacial characteristics, hyperextensible skin, joint laxity, kyphoscoliosis, arachnodactyly, inguinal hernia, and diverticulosis associated with biallelic pathogenic variants in EFEMP1 have been previously described in four patients. Genome sequencing on a proband and her mother with comparable phenotypic features revealed that both patients were heterozygous for a stop-gain variant c.1084C>T (p.Arg362*). Complementary RNA-seq on fibroblasts revealed significantly reduced levels of mutant EFEMP1 transcript. Considering the absence of other molecular explanations, we extrapolated that EFEMP1 could be the cause of the patient's phenotypes. Furthermore, nonsense-mediated decay was demonstrated for the mutant allele as the principal mechanism for decreased levels of EFEMP1 mRNA. We provide strong clinical and genetic evidence for the haploinsufficiency of EFEMP1 due to nonsense-medicated decay to cause severe kyphoscoliosis, generalized hypermobility of joints, high and narrow arched palate, and potentially severe diverticulosis. To the best of our knowledge, this is the first report of an autosomal dominant EFEMP1-associated hereditary connective tissue disorder and therefore expands the phenotypic spectrum of EFEMP1 related disorders.

Indexed as

Connective Tissue DiseasesExtracellular Matrix ProteinsHaploinsufficiencyMarfan SyndromePhenotypeAdultAllelesChildFemaleGenetic Predisposition to DiseaseHumansMaleMutationNonsense Mediated mRNA DecayPedigreeEFEMP1 protein, humanExtracellular Matrix ProteinsEFEMP1haploinsufficiencyhereditary connective tissue disordernonsense‐mediated decay

Identifiers

PMID38348595
PMCPMC11060917
OpenAlexW4391785652

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.