Evidence map›Paper›PMID 29797497›Full record

ArticleAmerican journal of medical genetics. Part A2018

Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibit.

Helga Rehder, Franco Laccone, Susanne G Kircher, Ralf L Schild, Christiane Rapp, Rainer Bald, Bernt Schulze, Jana Behunova, Juergen Neesen, Katharina Schoner

Open access · hybridAbstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part A, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 94% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. A Stop-gain Variant c.220C>T (p.(Gln74*)) inThe Yale journal of biology and medicine · 2023
    Review
  5. 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

10 authors at 6 institutions in 3 countries.

Helga RehderInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-5215-623X
Franco LacconeInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Susanne G KircherInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Ralf L SchildDepartment of Obstetrics, Diacovere Friederikenstift, Hannover, Germany.
Christiane RappDepartment of Praenatal Medicine, Klinikum Oldenburg, Oldenburg, Germany.
Rainer BaldClinic of Gynaecology and Obstetrics, Klinikum Leverkusen, Leverkusen, Germany.
Bernt SchulzePractice for Human Genetics, Hannover, Germany.
Jana BehunovaInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Juergen NeesenInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria.
Katharina SchonerInstitute of Pathology, Philipps University of Marburg, Marburg, Germany.
Medical University of Vienna · ATPhilipps University of Marburg · DECenter for Human Genetics · USHannover Re (Germany) · DEKlinikum Leverkusen · DEKlinikum Oldenburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Piepkorn type of lethal osteochondrodysplasia (POCD) is a rare and lethal dwarfing condition. Four cases have been reported to date. The characteristic features are distinctly shortened "flipper-like" limbs, polysyndactyly, excessive underossification, especially of the limb bones and vertebrae, and large (giant) chondrocytes in the cartilaginous bone primordia. These characteristics allowed the diagnosis of Piepkorn type of osteochondrodysplasia in four new cases, three fetuses of 15 to 22 weeks and one 106-year-old museum exhibit. Piepkorn type of osteochondrodysplasia has been assigned to the giant cell chondrodysplasias such as atelosteogenesis type 1 (AO1) and boomerang dysplasia (BD). Analysis of the Filamin B gene in 3p14.3, which is associated with these disorders, allowed the identification of the first FLNB mutations in Piepkorn type of osteochondrodysplasia. The heterozygous missense mutations, found in the three fetuses, were located in exons 28 and 29, encoding the immunoglobulin-like repeat region R15, one of three mutational hot spots in dominant FLNB-related skeletal disorders. Direct preparations and alcian blue staining revealed single upper and lower arm and leg bone primordia, preaxial oligodactyly, and polysyndactyly with complete fusion and doubling of the middle and end phalanges II-V to produce eight distal finger rays. Considering the unique clinical features and the extent of underossification, Piepkorn type of osteochondrodysplasia can be regarded as a distinct entity within the AO1-BD-POCD continuum.

Indexed as

MutationAdultDwarfismExhibitions as TopicFaciesFemaleFetal DiseasesFilaminsHumansMaleMiddle AgedOsteochondrodysplasiasPrognosisFilaminsFLNB protein, humanatelosteogenesis type 1boomerang dysplasiafetal skeletal dysplasiasFLNBPiepkorn type of osteochondrodysplasiaXY sex reversal

Identifiers

PMID29797497
PMCPMC6585644
OpenAlexW2804976417

What OpenQuestion holds

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LicenceCC BY-NC
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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.