Literature DB >> 7970943

Craniofacial morphology of spinal muscular atrophy.

K Houston1, P H Buschang, S T Iannaccone, N S Seale.   

Abstract

Spinal muscular atrophy (SMA) is the second most common neuromuscular disease of childhood. It is the most common fatal recessive neuromuscular disease. This study is the first to evaluate the craniofacial growth of SMA patients. The results pertain to a sample of 25 SMA patients, between 5 and 32 y of age, who were case matched with unaffected normal controls. Group differences for 25 measures, derived from tracings of standardized cephalometric radiographs, were evaluated using multivariate analysis of variance. The SMA group showed excessive vertical development, particularly of the lower face. They demonstrated relatively larger anterior than posterior facial heights, due in part to a smaller cranial base angulation and a more anteriorly positioned mandibular ramus. Anteroposterior skeletal discrepancies of SMA patients, due to the combined effects of a protrusive maxilla and a retrusive mandible, were moderate. The interincisal angle of the SMA group was smaller than normal, due primarily to proclined maxillary incisors. Relative to palatal length, the SMA group had smaller anterior cranial base and mandibular corpus lengths. These results suggest abnormal craniofacial growth patterns of SMA patients. The etiology of the observed abnormalities seems to be complex and multifaceted, but attention to the treatment of malocclusion may be important for optimal nutrition and respiratory function.

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Year:  1994        PMID: 7970943     DOI: 10.1203/00006450-199408000-00020

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  5 in total

1.  Noninvasive treatment strategy for swallowing problems related to prolonged nonoral feeding in spinal muscular atrophy type II.

Authors:  Tae-Hyun Cha; Duck-Won Oh; Jae-Hun Shim
Journal:  Dysphagia       Date:  2010-01-20       Impact factor: 3.438

2.  Conservative care of temporomandibular joint disorder in a 35-year-old patient with spinal muscular atrophy type III: a case study.

Authors:  Sébastien Houle; Martin Descarreaux
Journal:  J Chiropr Med       Date:  2009-12

3.  SMN-deficient cells exhibit increased ribosomal DNA damage.

Authors:  Evangelia Karyka; Nelly Berrueta Ramirez; Christopher P Webster; Paolo M Marchi; Emily J Graves; Vinay K Godena; Lara Marrone; Anushka Bhargava; Swagat Ray; Ke Ning; Hannah Crane; Guillaume M Hautbergue; Sherif F El-Khamisy; Mimoun Azzouz
Journal:  Life Sci Alliance       Date:  2022-04-19

4.  Use of Facial Morphology to Determine Nutritional Status in Older Adults: Opportunities and Challenges.

Authors:  Wesley Tay; Rina Quek; Bhupinder Kaur; Joseph Lim; Christiani Jeyakumar Henry
Journal:  JMIR Public Health Surveill       Date:  2022-07-18

Review 5.  Dysphagia Phenotypes in Spinal Muscular Atrophy: The Past, Present, and Promise for the Future.

Authors:  Katlyn Elizabeth McGrattan; Robert J Graham; Christine J DiDonato; Basil T Darras
Journal:  Am J Speech Lang Pathol       Date:  2021-04-06       Impact factor: 2.408

  5 in total

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