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Management of unilateral temporomandibular joint ankylosis & orthomorphic correction in a patient with Marfan syndrome: A rare case report

INTRODUCTION: Marfan syndrome (MFS) is a disorder of the connective tissue that is inherited in an autosomal dominant fashion and is caused by mutations in the gene coding for fibrillin-1 (FBN1). This condition commonly affects the skeletal system, pulmonary system, ocular system and the cardiovascu...

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Detalles Bibliográficos
Autores principales: Rudagi, B.M., Rishabh, Jain, Arif, Merchant, Namrata, Chourasia, Shahbaaz, Naikwade, Gaurav, Bhavar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7508685/
https://www.ncbi.nlm.nih.gov/pubmed/32950946
http://dx.doi.org/10.1016/j.ijscr.2020.09.033
Descripción
Sumario:INTRODUCTION: Marfan syndrome (MFS) is a disorder of the connective tissue that is inherited in an autosomal dominant fashion and is caused by mutations in the gene coding for fibrillin-1 (FBN1). This condition commonly affects the skeletal system, pulmonary system, ocular system and the cardiovascular system. Surgical intervention is often needed to correct the various deformities affecting the patients to restore the function, improving the patient’s aesthetic appearance and quality of life. PRESENTATION OF CASE: It’s a rare case report of a young male patient suffering through unilateral temporomandibular joint ankylosis, obstructive sleep apnea and unaesthetic appearance while being a case of Marfan syndrome. DISCUSSION: This paper highlights the various surgical procedures undertaken to correct the deformities affecting the individual and improving the overall health of the patient. CONCLUSION: Our patient’s management shows the necessity of a multidisciplinary, multi factorial and multi-faceted approach with early visual identification and diagnosis.