Evidence map›Paper›PMID 19609940›Full record

ReviewPrenatal diagnosis2009

Genetic considerations in the prenatal diagnosis of overgrowth syndromes.

Neeta Vora, Diana W Bianchi

Open access · bronzeAbstract readReview
In one paragraph

Review in Prenatal diagnosis, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Extremity anomalies associated with Robinow syndrome.American journal of medical genetics. Part A · 2021
    Article
  8. Review
  9. Review
  10. Fetal megacystis: a lot more than LUTO.Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology · 2019
    Article
  11. Co-occurrence of a maternally inheritedCold Spring Harbor molecular case studies · 2018
    Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Neeta VoraDivision of Genetics, Department of Pediatrics, Department of Obstetrics, Floating Hospital for Children and Tufts Medical Center, Boston, MA 02111, USA.
Diana W Bianchi
Tufts Children's Hospital · US

Funding

Physician & Scientist Training in Developmental GeneticsT32HD049341 · NICHD · TUFTS MEDICAL CENTER · PI BIANCHI, DIANA W. · 2006 to 2010
$1.4M
NICHD NIH HHS T32 HD049341
6 · The paper itself

Abstract

Large (>90%) for gestational age (LGA) fetuses are usually identified incidentally. Detection of the LGA fetus should first prompt the provider to rule out incorrect dates and maternal diabetes. Once this is done, consideration should be given to certain overgrowth syndromes, especially if anomalies are present. The overgrowth syndromes have significant clinical and molecular overlap, and are associated with developmental delay, tumors, and other anomalies. Although genetic causes of overgrowth are considered postnatally, they are infrequently diagnosed prenatally. Here, we review prenatal sonographic findings in fetal overgrowth syndromes, including Pallister-Killian, Beckwith-Wiedemann, Sotos, Perlman, and Simpson-Golabi-Behmel. We also discuss prenatal diagnosis options and recurrence risks.

Indexed as

AlgorithmsBeckwith-Wiedemann SyndromeChromosome AberrationsDiagnosis, DifferentialGenetic TestingGrowth DisordersHumansPrenatal DiagnosisSyndrome

Identifiers

PMID19609940
PMCPMC4426974
OpenAlexW2079151231

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.