Einloggen

Thematische Bibliographien / Dolichocephaly

Auswahl der wissenschaftlichen Literatur zum Thema „Dolichocephaly“

Autor: Grafiati

Veröffentlicht am 25. Juli 2024

Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an

Wählen Sie eine Art der Quelle aus:

Inhaltsverzeichnis

Zeitschriftenartikel
Buchteile
Konferenzberichte

Machen Sie sich mit den Listen der aktuellen Artikel, Bücher, Dissertationen, Berichten und anderer wissenschaftlichen Quellen zum Thema "Dolichocephaly" bekannt.

Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.

Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.

Zeitschriftenartikel zum Thema "Dolichocephaly"

1

Beckett, Joel S., Miles Jackson Pfaff, Michael Diluna und Derek M. Steinbacher. „Dolichocephaly Without Sagittal Craniosynostosis“. Journal of Craniofacial Surgery 24, Nr. 5 (September 2013): 1713–15. http://dx.doi.org/10.1097/scs.0b013e3182a12ece.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

2

Ben-Ami, M., E. Katzuni und A. Koren. „Imerslund Syndrome with Dolichocephaly“. Pediatric Hematology and Oncology 7, Nr. 2 (Januar 1990): 177–81. http://dx.doi.org/10.3109/08880019009033388.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

3

McManus, Beth, und Philip Capistran. „A Case Presentation of Early Intervention with Dolichocephaly in the NICU: Collaboration Between the Primary Nursing Team and the Developmental Care Specialist“. Neonatal Network 27, Nr. 5 (September 2008): 307–15. http://dx.doi.org/10.1891/0730-0832.27.5.307.

Der volle Inhalt der Quelle

Annotation:

Dolichocephaly, narrow width and long anterior-posterior cranial distance, is more commonly seen in preterm than in term infants. It seems to persist after NICU discharge and may be a marker for adverse neurodevelopment. This article reports a case of cranial molding in one extremely low birth weight infant. He was placed on a viscoelastic mattress and a twice weekly developmental care program. Cranial molding was measured using the cranial index (CI), a ratio of width to length. Initially, the patient presented with dolichocephaly (CI = 72 percent). By week 2, CI measurements approached normal limits (CI = 75 percent). When placed on continuous positive airway pressure, the infant presented with substantial dolichocephaly (CI = 66.7 percent). Following position changes to midline, CI measurements continued to improve and remained within normal limits until discharge. This dual-element program was feasible, acceptable to parents and staff, and may be effective for identifying and managing dolichocephaly.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

4

Modi, Rishi N., Caitlyn C. Belza, George N. Kamel, Ryan M. McKee, Mary K. Carbullido und Amanda A. Gosman. „Delayed Presentation of Sagittal Suture Craniosynostosis“. Annals of Plastic Surgery 88, Nr. 4 (Mai 2022): S351—S356. http://dx.doi.org/10.1097/sap.0000000000003137.

Der volle Inhalt der Quelle

Annotation:

Background Sagittal craniosynostosis typically presents as dolichocephaly or less frequently as clinocephaly, a “saddle-shaped” phenotype. This project aimed to characterize clinically relevant differences between sagittal synostosis phenotypes and examine the etiology of the delay in presentation. Methods An institutional review board–approved retrospective review was performed from January 1999 to November 2018 at a single institution. Analyses examined correlations between subphenotype, time of presentation, minor suture fusion, developmental delay, and operative technique. Results One hundred sixty patients diagnosed with single-suture sagittal craniosynostosis were identified. A total of 30.6% had a saddle phenotype (n = 49) and 69.4% had dolichocephaly (n = 111). Patients with the saddle phenotype were more likely to present with a developmental delay and to have at least 1 minor suture fused than patients with dolichocephaly were. Patients with the saddle phenotype presented for surgery at an older age and were more likely to undergo open cranial vault repair, with increased blood loss, higher transfusion volume, and longer time. Conclusions This study highlights clinical differences in sagittal craniosynostosis phenotypes and shows that developmental delay is an initial presentation of the saddle phenotype. The saddle phenotype also correlated with fusion of the minor squamous and sphenoid sutures. The link between developmental delay and minor suture fusion was notable and should be explored with a larger sample size. Patients with saddle synostosis present for surgery at an older age than patients with dolichocephaly and therefore are more likely to receive open cranial vault repair, with a taxing intraoperative experience characterized by increased blood loss, increased transfusions, and longer operation time.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

5

Yu, Dongyi, Shuo Li, Qi Liu und Kai Zhang. „Novel chromosomal microduplications associated with dolichocephaly craniosynostosis“. Medicine 96, Nr. 49 (Dezember 2017): e8729. http://dx.doi.org/10.1097/md.0000000000008729.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

6

Gaibov, S. S., E. V. Zakharchyk und D. P. Vorobjov. „Morphometric analysis of the structures of the skull according to computed tomography data in children in norm and in dolichocephaly“. Сибирский научный медицинский журнал 43, Nr. 4 (29.08.2023): 65–69. http://dx.doi.org/10.18699/ssmj20230406.

Der volle Inhalt der Quelle

Annotation:

There is an increased interest in the problem of helping children with skull deformities that occur due to premature closure of cranial sutures and the development of craniosynostosis. Assessment of cranial dysmorphism in skull deformities is often subjective and remains a challenge. Morphometric studies are a significant section that is poorly covered in modern scientific, practical and reference medical literature.Material and methods. The analysis of the data of craniometric measurements, of cephalic index (CI) according to the results of computed tomography in 24 children with dolichocephaly (14 boys, 10 girls) at the age of 7.4 ± 3.2 months (2–12 months) and in the control group of 25 children (15 boys, 9 girls) at the age of 7.2 ± 4.8 months (2–12 months).Results. The data showed significant differences in children in norm and in dolichocephaly. CI shows the ratio of the linear dimensions of the skull in normal and dolichocephaly. The most significant differences were revealed when assessing the distances G-Op, CG-TS, CG-MAI, MAI-MAI, Zg-Zg, Ec-Ec, Br-Ba. CG-TS, CG-MAI, MAI-MAI, Br-Ba reflect deformation of the skull base, and Zg-Zg, Ec-Ec – deformation of the facial skeleton in dolichocephaly.Conclusions. A comprehensive morphometric analysis of the skull structures based on precise anatomical landmarks demonstrated objective differences in the morphology of the skull in children with normal conditions and with dolichocephaly. The data indicate the importance of a comprehensive assessment of changes in the skull for all forms of the skull. Carrying out such an analysis is important for understanding all morphological changes in the skull in health and disease.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

7

Celentano, Claudio, Raffaella Zannolli, Sabrina Buoni, Sergio Domizio, Giuseppe Sabatino, Cesare Colosimo, Anita Saponari et al. „Classical lissencephaly associated with dolichocephaly, hair and nail defect“. Brain and Development 28, Nr. 6 (Juli 2006): 392–94. http://dx.doi.org/10.1016/j.braindev.2005.10.011.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

8

Levine, D., S. Kilpatrick, N. Damato und P. W. Callen. „Dolichocephaly and oligohydramnios in preterm premature rupture of the membranes.“ Journal of Ultrasound in Medicine 15, Nr. 5 (Mai 1996): 375–79. http://dx.doi.org/10.7863/jum.1996.15.5.375.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

9

Kochuvareed Mampilly, Tomy, George Tomy Mampilly, Neeradha Chandramohan, Murugan Velayutham, Jayesh Sheth, Frenny Sheth und Vijayalakshmy Janaki. „Prenatal dolichocephaly: Sign of trouble? –A variant of Miller–Dieker syndrome“. Fetal and Pediatric Pathology 32, Nr. 4 (10.01.2013): 308–11. http://dx.doi.org/10.3109/15513815.2012.754529.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

10

Peat, Jennifer, William Malcolm, P. Smith, Kimberley Fisher, Ricki Goldstein und Dana McCarty. „Dolichocephaly in Preterm Infants: Prevalence, Risk Factors, and Early Motor Outcomes“. American Journal of Perinatology 34, Nr. 04 (02.09.2016): 372–78. http://dx.doi.org/10.1055/s-0036-1592128.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

Mehr Quellen

Buchteile zum Thema "Dolichocephaly"

1

„Dolichocephalic“. In Encyclopedic Dictionary of Archaeology, 398. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-58292-0_40358.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

2

„dolichocephal, n.“ In Oxford English Dictionary. 3. Aufl. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/7461363099.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

3

„dolichocephalic, adj.“ In Oxford English Dictionary. 3. Aufl. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/2771990103.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

4

Damasio, Hanna. „Exterior Description of a Normal Dolichocephalic Brain“. In Human Brain Anatomy in Computerized Images, 11–30. Oxford University Press, 2005. http://dx.doi.org/10.1093/acprof:oso/9780195165616.003.0002.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

Konferenzberichte zum Thema "Dolichocephaly"

1

Silva, Bruno Custódio, Guilherme Parmigiani Bobsin, Raquel dos Santos Ramos, Tatiane Andressa Gasparetto, Vivianne Amanda do Nascimento, Paulo Ricardo Gazzola Zen und Rafael Fabiano Machado Rosa. „Clinical and neurological findings of a patient with a complex chromosome 5 alteration“. In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.080.

Der volle Inhalt der Quelle

Annotation:

Context: Inversion-duplication-deletion (invdupdel) involving the short arm of chromosome 5 is considered a complex and extremely rare alteration. Case report: A female patient was born prematurely at 32 weeks and was delivered by cesarean section, weighing 2,086 grams, with an Apgar score in the fifth minute of 7. After birth, she needed invasive mechanical ventilation. A nasofibrolaryngoscopy was performed, which revealed the rear projection of the tongue base. The speech-language evaluation showed a swallowing disorder. The patient needed to be tracheostomized and evolved with episodes of cardiorespiratory arrest. A zone 2 of immaturity was identified in both eyes. Then, gastroesophageal reflux was also diagnosed. Cerebral ultrasound showed moderate lateral ventricles dilation. High resolution GTG-banding karyotype identified an inverted and partial duplication of the chromosome’s 5 short arm, with a probable deletion of its distal segment: 46,XX,invdup(5) (p13.3->p15.33:: p15.33->qter) [23]. The parents’ karyotype was normal. At 2 months, the patient had dolichocephaly; bitemporal narrowing; hypertelorism; and down slanting palpebral fissures with blepharophimosis; low-set and posteriorly rotated ears; leftover skin at neck and bilateral plantar creases between the first, second and third toes. Conclusions: Invdupdel of the short arm of chromosome 5 is a very rare chromosomal alteration. Neurological findings seem to be part of its clinical manifestations, especially dilated lateral ventricles. More reports will be essential for understanding its clinical spectrum.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

Wir bieten Rabatte auf alle Premium-Pläne für Autoren, deren Werke in thematische Literatursammlungen aufgenommen wurden. Kontaktieren Sie uns, um einen einzigartigen Promo-Code zu erhalten!