Evidence map›Paper›PMID 18551360›Full record

ArticleJournal of genetic counseling2008

Genetic counseling in southern Iran: consanguinity and reason for referral.

Mohsen Fathzadeh, Mohammad Ali Babaie Bigi, Masood Bazrgar, Majid Yavarian, Hamid Reza Tabatabaee, Seyed Mohammad Akrami

Abstract read
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In one paragraph

Article in Journal of genetic counseling, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The status ofMedical journal of the Islamic Republic of Iran · 2019
    Article
  6. Article
  7. The genetic background of Southern Iranian couples before marriage.Balkan journal of medical genetics : BJMG · 2016
    Article
  8. Article
  9. Mutation analysis of the CYP21A2 gene in the Iranian population.Genetic testing and molecular biomarkers · 2012
    Article
  10. 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

6 authors.

Mohsen FathzadehHuman Genetic Rresearch Group, Iranian Academic Center for Education, Culture & Research, Fars Province Branch, Shiraz, Iran. fathzadehm@sums.ac.ir
Mohammad Ali Babaie Bigi
Masood Bazrgar
Majid Yavarian
Hamid Reza Tabatabaee
Seyed Mohammad Akrami

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Population based genetic counseling that promotes public health goals is an appropriate health care service. The genetic counseling center in Shiraz, southern Iran serves most of the clients in the region. During a 4-year period, 2,686 couples presented for genetic counseling. Data files revealed that 85% had consanguineous relationships (1.5% double first cousin, 74% first cousin, 8% second cousin, 1.5% beyond second cousin). Most prevalent reasons for referral were premarital counseling (80%), with 89% consanguinity, followed by preconception (12%), postnatal (7%), and prenatal counseling (1%). The most common abnormalities in probands or relatives were intellectual and developmental disabilities, hearing loss/impairment, and neuromuscular dystrophies. Family history of medical problem(s) and/or consanguinity was the main indication for referral in nearly every family. Premarital consanguinity poses unique challenges and opportunities. There is considerable opportunity for genetic counseling and education for couples in this population. The tradition of consanguinity, which is likely to persist in Iran, requires multidisciplinary agreement regarding the appropriate process of genetic counseling. Effective genetic counseling in Iran hinges on inclusion of data from genetic counseling services in national genomic and epidemiologic research programs.

Indexed as

ConsanguinityGenetic CounselingReferral and ConsultationAdolescentAdultAgedChildChild, PreschoolFemaleGenetic Diseases, InbornHumansInfantInfant, NewbornIranMaleMiddle Aged

Identifiers

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Registered trials

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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.