Evidence map›Paper›PMID 26843738›Full record

ArticleMedical archives (Sarajevo, Bosnia and Herzegovina)2015

Genetic Profile of Patients with Familial Mediterranean Fever (FMF): Single Center Experience at King Hussein Medical Center (KHMC).

Lana Ayesh Habahbeh, Mansour Al Hiary, Samar F Al Zaben, Asim Al-Momani, Rame Khasawneh, Mervat Abu Mallouh, Hayab Farahat

Open access · greenAbstract read
In one paragraph

Article in Medical archives (Sarajevo, Bosnia and Herzegovina), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  9. Frequencies of theBalkan journal of medical genetics : BJMG · 2021
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  10. Spectrum ofMedical sciences (Basel, Switzerland) · 2020
    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

7 authors at 1 institution in 1 country.

Lana Ayesh HabahbehDepartment of Pathology, King Hussein Medical Center, Amman, Jordan.
Mansour Al HiaryDepartment of Pathology, King Hussein Medical Center, Amman, Jordan.
Samar F Al ZabenDepartment of Pathology, King Hussein Medical Center, Amman, Jordan.
Asim Al-MomaniDepartment of Pathology, King Hussein Medical Center, Amman, Jordan.
Rame KhasawnehDepartment of Pathology, King Hussein Medical Center, Amman, Jordan.
Mervat Abu MallouhDepartment of Pathology, King Hussein Medical Center, Amman, Jordan.
Hayab FarahatDepartment of Pathology, King Hussein Medical Center, Amman, Jordan.
King Hussein Medical Center · JO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo describe the spectrum of genetic mutations in patients with clinical diagnosis of Familial Mediterranean Fever.

methodThis is a retrospective study of 3359 sera samples for patient with clinical diagnosis of FMF, over a period of 6 years. The samples were tested for 12 mutations of the MEFV gene by PCR& hybridization of the PCR product with Probes immobilized as an array of panel lines.

resultsA total of 1868 (55.6%) samples were found negative, and one or more mutations were detected in 1491 (44.4%) distributed along the mutations. Of the positive results, the Frequency of the mutations was as follows, the M694V was the most common mutation 30%, followed by E 148Q 21.5%, V 726 A 20%, M6801 G/C 9%, M6941 8.3%, P369s 3.7%, A744S 3.1% and 4.2% among the 4 remaining mutations.

conclusionFrequency of common mutations in our study show similar results in comparisons with Mediterranean countries like Egypt, Turkey, and Syria with the most common mutation in our study being M694V followed by E148 Q.

Indexed as

Familial Mediterranean FeverHeterozygoteHomozygoteHumansJordanMutationPolymerase Chain ReactionPyrinRetrospective StudiesMEFV protein, humanPyrinFMFgenotypeKing Hussein Medical Center

Identifiers

PMID26843738
PMCPMC4720465
OpenAlexW2269520141

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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.