Literature DB >> 14623689

Thickness and histologic and histochemical properties of the superior pharyngeal constrictor muscle in velocardiofacial syndrome.

Shane Zim1, Robert Schelper, Robert Kellman, Sherard Tatum, Robert Ploutz-Snyder, Robert Shprintzen.   

Abstract

BACKGROUND: Velocardiofacial syndrome (VCFS) is one of the most common multiple anomaly syndromes in humans. Pharyngeal hypotonia, one of the most common findings in VCFS, contributes to hypernasal speech, which occurs in approximately 75% of individuals with VCFS.
OBJECTIVE: To evaluate the thickness and histologic and histochemical properties of the superior pharyngeal constrictor (SPC) muscle in patients with VCFS to determine whether a muscle abnormality exists that might contribute to the hypotonia seen in these patients. Subjects The SPC muscle thickness in 26 VCFS patients (18 male and 8 female; age range, 3-29 years) was compared with SPC muscle thickness in age- and sex-matched controls using magnetic resonance images. The histologic and histochemical properties of the SPC muscle in 9 VCFS patients (6 male and 3 female; age range, 4-12 years) were compared with SPC muscle in 3 adult cadavers without VCFS (all male; age range, 80-86 years) using specimens obtained during pharyngeal flap surgery.
RESULTS: The thickness of the SPC muscle was significantly less in patients with VCFS (2.03 mm) than in patients without VCFS (2.85 mm). The SPC muscle contained a significantly greater proportion of type 1 fibers in patients with VCFS (27.7%) than in adults without VCFS (17.9%), and the diameter of the type 1 fibers was significantly smaller in patients with VCFS (21.6 micro m) than in adults without VCFS (26.6 micro m).
CONCLUSIONS: Differences in the thickness and histologic and histochemical properties of the SPC muscle found in patients with VCFS compared with individuals without VCFS may offer insight into the cause of pharyngeal hypotonia and hypernasal speech seen in these patients.

Entities:  

Mesh:

Year:  2003        PMID: 14623689     DOI: 10.1001/archfaci.5.6.503

Source DB:  PubMed          Journal:  Arch Facial Plast Surg        ISSN: 1521-2491


  10 in total

Review 1.  Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology.

Authors:  Thomas M Maynard; Irene E Zohn; Sally A Moody; Anthony-S LaMantia
Journal:  Annu Rev Neurosci       Date:  2020-02-26       Impact factor: 12.449

Review 2.  Head and neck manifestations of 22q11.2 deletion syndromes.

Authors:  Tal Marom; Yehudah Roth; Abraham Goldfarb; Udi Cinamon
Journal:  Eur Arch Otorhinolaryngol       Date:  2011-08-23       Impact factor: 2.503

3.  Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: a phenotype correlation study.

Authors:  Marcia A Friedman; Nathanial Miletta; Cheryl Roe; Dongliang Wang; Bernice E Morrow; Wendy R Kates; Anne Marie Higgins; Robert J Shprintzen
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2011-07-18       Impact factor: 1.675

Review 4.  Velo-cardio-facial syndrome: 30 Years of study.

Authors:  Robert J Shprintzen
Journal:  Dev Disabil Res Rev       Date:  2008

5.  Tbx1 is required autonomously for cell survival and fate in the pharyngeal core mesoderm to form the muscles of mastication.

Authors:  Ping Kong; Silvia E Racedo; Stephania Macchiarulo; Zunju Hu; Courtney Carpenter; Tingwei Guo; Tao Wang; Deyou Zheng; Bernice E Morrow
Journal:  Hum Mol Genet       Date:  2014-04-04       Impact factor: 6.150

6.  Age-related composition changes in swallowing-related muscles: a Dixon MRI study.

Authors:  Yuta Nakao; Yuki Uchiyama; Kosuke Honda; Taiji Yamashita; Shota Saito; Kazuhisa Domen
Journal:  Aging Clin Exp Res       Date:  2021-04-26       Impact factor: 3.636

7.  Histology of the pharyngeal constrictor muscle in 22q11.2 deletion syndrome and non-syndromic children with velopharyngeal insufficiency.

Authors:  Josine C C Widdershoven; Nicole E Spruijt; Wim G M Spliet; Corstiaan C Breugem; Moshe Kon; Aebele B Mink van der Molen
Journal:  PLoS One       Date:  2011-06-28       Impact factor: 3.240

8.  A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome.

Authors:  Jennifer C Fuchs; Jennifer F Linden; Antonio Baldini; Abigail S Tucker
Journal:  Hum Mol Genet       Date:  2014-12-01       Impact factor: 6.150

9.  Estimates of the Prevalence of Speech and Motor Speech Disorders in Youth With 22q11.2 Deletion Syndrome.

Authors:  Adriane L Baylis; Lawrence D Shriberg
Journal:  Am J Speech Lang Pathol       Date:  2019-02-21       Impact factor: 2.408

10.  Characteristics of velopharyngeal dysfunction in 22q11.2 deletion syndrome: a retrospective case-control study.

Authors:  Sebastiano Failla; Peng You; Chandheeb Rajakumar; Anne Dworschak-Stokan; Philip C Doyle; Murad Husein
Journal:  J Otolaryngol Head Neck Surg       Date:  2020-07-31
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.