| Dental treatment of Marfan syndrome. With regard to a case. | |
| | |
MedLine Citation:
|
PMID: 20711146 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
|
Marfan syndrome (MS) is the most common dominant autosomic genetic disorder of the connective tissue. It has a reported incidence of 1 per each 5000 individuals without any distinction of gender or ethnicity. This pathology's diagnosis is mainly based on physical characteristics, presenting three main different symptomatic charts: neonatal Marfan, infant Marfan and classical Marfan. The mayor characteristic of these patients consists of an exaggerated length of the upper and lower limbs, hyperlaxity, scoliosis, alterations in the cardiovascular and pulmonary systems and atypical bone overgrowth. The individual implied in the present investigation concerned to a 14 year old male patient presenting multiple mouth lesions and dental alterations, attended in the Department of Pediatric Dentistry degree at the Dentistry School in the Santa Maria University. The patient has been treated following the necessary considerations required according to his systemic compromise under oral premedication for decrease the anxiety and make easier the behavior management. The patient with MS has multiple oral decrease that may be diagnosed as treated on time to increase the life quality of the patient. |
| | |
Authors:
|
Mariana-Carolina Morales-Chávez; María-Verónica Rodríguez-López |
Related Documents
:
|
10522336 - New-onset headache in an adolescent with mass syndrome. 11922446 - Multiple valvar replacements for hypereosinophilic syndrome. 15509216 - Primary carcinoid tumor of the bilateral testis associated with carcinoid syndrome. 19117906 - Clinical and molecular study of 320 children with marfan syndrome and related type i fi... 3281216 - Kawasaki syndrome. 519896 - The aarskog (facio-digito-genital) syndrome. |
Publication Detail:
|
Type: Case Reports; Journal Article Date: 2010-11-01 |
Journal Detail:
|
Title: Medicina oral, patología oral y cirugía bucal Volume: 15 ISSN: 1698-6946 ISO Abbreviation: Med Oral Patol Oral Cir Bucal Publication Date: 2010 Nov |
Date Detail:
|
Created Date: 2010-11-02 Completed Date: 2011-03-30 Revised Date: 2011-04-06 |
Medline Journal Info:
|
Nlm Unique ID: 101231694 Medline TA: Med Oral Patol Oral Cir Bucal Country: Spain |
Other Details:
|
Languages: eng Pagination: e859-62 Citation Subset: D; IM |
Affiliation:
|
Magister in Patients with Special needs, Valencia University, Spain. macamocha@hotmail.com |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
Adolescent Humans Male Marfan Syndrome / complications* Tooth Diseases / etiology*, surgery* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Use of Bichat's buccal fat pad for the sealing of orosinusal communications. A presentation of 8 cas...
Next Document: Altered passive eruption (APE): a little-known clinical situation.