Evidence map›Paper›PMID 39176338›Full record

ArticleCureus2024

A Case of Fibular Aplasia-Tibial Campomelia-Oligosyndactyly (FATCO) Syndrome Associated With Split Hand/Foot Syndrome With Long Bone Deficiency (SHFLD) and Review of the Literature.

Theodora-Eleftheria Deftereou, Vaya R Karapepera, Christina Angelika Alexiadi, Stylianos Tologkos, Vasiliki Papadatou, Georgios Alexiadis, Dimitrios Karamanidis, Lambropoulou Maria

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In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Theodora-Eleftheria DeftereouLaboratory of Histology-Embryology, Democritus University of Thrace, Alexandroupolis, GRC.
Vaya R KarapeperaENT Clinic, General Hospital of Ioannina "G. Hatzikosta", Ioannnina, GRC.
Christina Angelika AlexiadiLaboratory of Histology-Embryology, Democritus University of Thrace, Alexandroupolis, GRC.
Stylianos TologkosLaboratory of Histology-Embryology, Democritus University of Thrace, Alexandroupolis, GRC.
Vasiliki PapadatouLaboratory of Histology-Embryology, Democritus University of Thrace, Alexandroupolis, GRC.
Georgios AlexiadisDepartment of Radiology, Private Radiodiagnostic Center, Alexandroupolis, GRC.
Dimitrios KaramanidisDepartment of Obstetrics and Gynecology, University General Hospital of Alexandroupolis, Alexandroupolis, GRC.
Lambropoulou MariaLaboratory of Histology-Embryology, Democritus University of Thrace, Alexandroupolis, GRC.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Split hand/foot malformation is a heterogeneous congenital disorder mainly presented with a median cleft of hands or/and feet. It can be associated with long bone aplasia, a syndrome also known as split hand/foot syndrome with long bone deficiency (SHFLD), which is a very rare condition. We report a very rare case of a male fetus with SHFLD syndrome combined with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome. FATCO syndrome is also an extremely infrequent congenital limb defect by itself. Based on our review of the literature, there appears to be no other FATCO case reported in Greece.

Indexed as

ectrodactylyfatcofibular aplasiashfldtibial campomelia

Identifiers

PMID39176338
PMCPMC11339580

What OpenQuestion holds

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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.