craniostenose em gêmeos: estudo genético craniostenosis in twins: a genetic study
Clicks: 130
ID: 222000
1968
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Popular Article
30.0
/100
130 views
13 readers
AI Quality Assessment
Not analyzed
Readership in this journal
PopularRanked #261 of 475 articles by views in communications in computer and information science
Most read
Least read
Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 475 in total.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
É relatada a ocorrência de formas clínicas diversas de craniostenose em gêmeos de sexo diferente. A menina apresentava obliteração completa da sutura coronaria e dos dois terços anteriores da sutura sagital; no menino a sutura sagital era a única afetada. O estudo genético mostrou que a craniostenose independe de aberrações cromossômicas, indicando ser transmitida por gens recessivos raros de natureza autossômica.
The occurrence of two clinical forms of craniostenosis in twins of different sex born to consanguineous parents is reported. The girl showed total fusion of the coronary suture; in the boy sagittal suture was the only one involved. The genetic study showed that the craniostenosis was not associated with chromosomal anomalies and was related to rare auto-somic recessive gens.
The occurrence of two clinical forms of craniostenosis in twins of different sex born to consanguineous parents is reported. The girl showed total fusion of the coronary suture; in the boy sagittal suture was the only one involved. The genetic study showed that the craniostenosis was not associated with chromosomal anomalies and was related to rare auto-somic recessive gens.
| Reference Key |
pereira1968arquivoscraniostenose
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | ;Walter Carlos Pereira;Nélio Garcia de Barros;Gilberto Machado de Almeida;Pedro Henrique Saldanha |
| Journal | communications in computer and information science |
| Year | 1968 |
| DOI |
DOI not found
|
| URL | |
| Keywords |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.