cytosine has been researched along with Craniosynostoses in 4 studies
Craniosynostoses: Premature closure of one or more CRANIAL SUTURES. It often results in plagiocephaly. Craniosynostoses that involve multiple sutures are sometimes associated with congenital syndromes such as ACROCEPHALOSYNDACTYLIA; and CRANIOFACIAL DYSOSTOSIS.
| Excerpt | Relevance | Reference |
|---|---|---|
| "In place of the typical craniosynostosis found in CFND, she presented with a superiorly displaced nasion and an anomalously positioned frontonasal suture." | 1.39 | Craniofrontonasal dysplasia: variability of the frontonasal suture and implications for treatment. ( Buchanan, EP; Correa, B; Hollier, LH; Weathers, WM; Wolfswinkel, EM, 2013) |
| "Myotonic dystrophy is considered a true dominant condition with no difference in the phenotype between heterozygous and homozygous cases." | 1.35 | Homozygous myotonic dystrophy with craniosynostosis. ( Cerghet, M; Mahbubul Huq, AH; Serajee, FJ; Tapos, D, 2008) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Wolfswinkel, EM | 1 |
| Weathers, WM | 1 |
| Correa, B | 1 |
| Buchanan, EP | 1 |
| Hollier, LH | 1 |
| Anderson, PJ | 1 |
| Netherway, DJ | 1 |
| Cox, TC | 1 |
| Roscioli, T | 1 |
| David, DJ | 1 |
| Cerghet, M | 1 |
| Tapos, D | 1 |
| Serajee, FJ | 1 |
| Mahbubul Huq, AH | 1 |
| Moko, SB | 1 |
| Blandin de Chalain, TM | 1 |
4 other studies available for cytosine and Craniosynostoses
| Article | Year |
|---|---|
Craniofrontonasal dysplasia: variability of the frontonasal suture and implications for treatment.
Topics: Child; Codon; Cranial Sutures; Craniofacial Abnormalities; Craniosynostoses; Cytosine; Ephrin-B1; Fe | 2013 |
Do Craniosynostosis syndrome phenotypes with both FGFR2 and TWIST mutations have a worse clinical outcome?
Topics: Acrocephalosyndactylia; Adenine; Adolescent; Arginine; Child, Preschool; Craniofacial Dysostosis; Cr | 2006 |
Homozygous myotonic dystrophy with craniosynostosis.
Topics: Alleles; Brain; Child, Preschool; Cranial Sutures; Craniosynostoses; Cytosine; DNA Mutational Analys | 2008 |
New Zealand Maori family with the pro250arg fibroblast growth factor receptor 3 mutation associated with craniosynostosis.
Topics: Arginine; Codon; Craniosynostoses; Cytosine; Exons; Female; Fibroblast Growth Factors; Frontal Bone; | 2001 |