Bibliografie tematiche / Dolichocephaly

Letteratura scientifica selezionata sul tema "Dolichocephaly"

Autore: Grafiati
Pubblicato: 25 luglio 2024

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Articoli di riviste sul tema "Dolichocephaly"

1

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

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2

Ben-Ami, M., E. Katzuni e A. Koren. "Imerslund Syndrome with Dolichocephaly". Pediatric Hematology and Oncology 7, n. 2 (gennaio 1990): 177–81. http://dx.doi.org/10.3109/08880019009033388.

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3

McManus, Beth, e 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, n. 5 (settembre 2008): 307–15. http://dx.doi.org/10.1891/0730-0832.27.5.307.

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

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Abstract (sommario):
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.
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Yu, Dongyi, Shuo Li, Qi Liu e Kai Zhang. "Novel chromosomal microduplications associated with dolichocephaly craniosynostosis". Medicine 96, n. 49 (dicembre 2017): e8729. http://dx.doi.org/10.1097/md.0000000000008729.

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Gaibov, S. S., E. V. Zakharchyk e 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, n. 4 (29 agosto 2023): 65–69. http://dx.doi.org/10.18699/ssmj20230406.

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Abstract (sommario):
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.
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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, n. 6 (luglio 2006): 392–94. http://dx.doi.org/10.1016/j.braindev.2005.10.011.

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8

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

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9

Kochuvareed Mampilly, Tomy, George Tomy Mampilly, Neeradha Chandramohan, Murugan Velayutham, Jayesh Sheth, Frenny Sheth e Vijayalakshmy Janaki. "Prenatal dolichocephaly: Sign of trouble? –A variant of Miller–Dieker syndrome". Fetal and Pediatric Pathology 32, n. 4 (10 gennaio 2013): 308–11. http://dx.doi.org/10.3109/15513815.2012.754529.

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10

Peat, Jennifer, William Malcolm, P. Smith, Kimberley Fisher, Ricki Goldstein e Dana McCarty. "Dolichocephaly in Preterm Infants: Prevalence, Risk Factors, and Early Motor Outcomes". American Journal of Perinatology 34, n. 04 (2 settembre 2016): 372–78. http://dx.doi.org/10.1055/s-0036-1592128.

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Più fonti

Capitoli di libri sul tema "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.

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"dolichocephal, n." In Oxford English Dictionary. 3a ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/7461363099.

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"dolichocephalic, adj." In Oxford English Dictionary. 3a ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/2771990103.

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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.

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Atti di convegni sul tema "Dolichocephaly"

1

Silva, Bruno Custódio, Guilherme Parmigiani Bobsin, Raquel dos Santos Ramos, Tatiane Andressa Gasparetto, Vivianne Amanda do Nascimento, Paulo Ricardo Gazzola Zen e 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.

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Abstract (sommario):
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.
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