Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Meghan Tracy"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 6, Pp n/a-n/a (2020)
Abstract Background To delineate sleep habits and problems in children with 22q11.2 deletion syndrome (22q11DS). Methods Thirty children, age 1–15 (mean 6.8) years, participated in the study, which was an internet‐based anonymous survey of parent
Externí odkaz:
https://doaj.org/article/40599d39ff424ad5bb8a97b86cc1cb46
Publikováno v:
Cureus.
Autor:
Susan Starling Hughes, M. Max Feldt, Lei Zhang, Jill M. Arganbright, Lauren E. Bartik, Alison E. Kaye, Meghan Tracy
Publikováno v:
American Journal of Medical Genetics Part A. 188:779-787
22q11.2 duplication syndrome has a frequency of ~1/700 in the intellectual disability population. Despite this frequency, there is limited information on the variable clinical presentation. Although the phenotype and incidence of congenital anomalies
Autor:
Jill M. Arganbright, Paul Bryan Hankey, Meghan Tracy, Srivats Narayanan, Janelle Noel-MacDonnell, David Ingram
Publikováno v:
Genes; Volume 13; Issue 12; Pages: 2187
Tonsillectomy is one of the most common procedures performed in children, however there are currently no published studies evaluating tonsillectomy in children with 22q11.2 deletion syndrome (22q11DS). With this study, our goal was to investigate the
Autor:
Jill M. Arganbright, Meghan Tracy, Max Feldt, Srivats Narayanan, Ashna Mahadev, Janelle Noel-MacDonnell
Publikováno v:
Genes; Volume 13; Issue 10; Pages: 1905
The guidelines for management of children with 22q11.2 deletion syndrome (22q11DS) highlight the risk for developing hypocalcemia after surgery and recommend monitoring calcium perioperatively. Despite this guidance, little has been published on post
Publikováno v:
International journal of pediatric otorhinolaryngology. 164
The internal carotid artery (ICA) lies in close anatomic proximity to the oropharynx and is at risk for injury in the instance of intraoral trauma. The objectives of this study are to describe the position of the ICA relative to the oropharynx and id
Publikováno v:
The Cleft Palate-Craniofacial Journal. 59:S28-S36
Objective: To determine the prevalence of, reasons for, and outcomes related to Child Protective Services (CPS) referral in an isolated and syndromic cleft lip/palate population. Design: Retrospective cohort study. Setting: Tertiary Children’s Hosp
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 163:111373
People with 22q11.2 deletion syndrome (22q11DS) can present with a wide variety of findings. Various airway anomalies have been described intermittently within this syndrome, but this feature has not been extensively investigated. Increased provider
Publikováno v:
International journal of pediatric otorhinolaryngology. 155
Invasive fungal rhinosinusitis (IFRS) is a potentially fatal disease that affects the severely immunocompromised and requires aggressive treatment. The objective of this study is to better describe predictors of biopsy positivity in patients at high
Publikováno v:
The Cleft Palate-Craniofacial Journal. 56:1096-1106
There is currently no recognized connection between the occurrence of cleft lip and/or palate (CL/P) and Wilms tumor (WT). A retrospective review of cleft team records (2001-2015) revealed 3 cases of children, all male, with concomitant diagnoses of