Evidence map›Paper›PMID 20878219›Full record

ArticleJournal of genetic counseling2011

Communication of genetic risk information to daughters in families with fragile X syndrome: the parent's perspective.

Allyn McConkie-Rosell, Jacqueline Del Giorno, Elizabeth Melvin Heise

Open access · bronzeAbstract read
In one paragraph

Article in Journal of genetic counseling, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

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  10. Developmental and behavioral pediatricians' attitudes toward screening for fragile X.American journal on intellectual and developmental disabilities · 2013
    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

3 authors at 1 institution in 1 country.

Allyn McConkie-RosellDivision of Medical Genetics, Department of Pediatrics, Duke University Health System, Box 103857, Durham, NC 27710, USA. allyn.mcconkie@duke.edu
Jacqueline Del Giorno
Elizabeth Melvin Heise
Duke University Health System · US

Funding

What about adolescence? Living with genetic riskR03HD044647 · NICHD · DUKE UNIVERSITY · PI MCCONKIE-ROSELL, ALLYN · 2004 to 2005
$154k
NICHD NIH HHS 5R03HD044647-02NICHD NIH HHS R03 HD044647
6 · The paper itself

Abstract

Parental approaches to communicating information about genetic disorders to their children may be an important determinant in how the children manage stress as well as their adjustment and adaptation to that information. We explored communication patterns through structured interviews with 46 parents of daughters who learned about their genetic risk status as minors. Three different levels of knowledge about fragile X syndrome were explored: 1) informing that it has been diagnosed in the family and is an inherited disorder, 2) informing about the possibility of a daughter being a carrier, and 3) if testing had been done, informing the daughter of her actual carrier status. Additionally, parental perceptions of their daughter's understanding of the information were explored along with frequency of discussions. We found that communication about genetic risk was initiated by the parents. Five disclosure patterns were identified with variations in style, content, and frequency of communication related to the information that was being disclosed. Aspects of resilient communication were present for all levels of disclosure; however, as the information became more personally relevant for the daughter such as disclosure about the possibility of "being a carrier" for fragile X syndrome and there was uncertainty regarding potential outcomes, the conversations included fewer resilient characteristics. Uncertainty about what and how to present information may negatively affect a parent's ability to include elements of resilient communication when disclosing genetic risk information.

Indexed as

Genetic Predisposition to DiseaseParent-Child RelationsCross-Sectional StudiesFemaleFragile X SyndromeGenetic Carrier ScreeningHumansMale

Identifiers

PMID20878219
PMCPMC3508506
OpenAlexW2041813050

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.