Marfan syndrome (MFS) is a type of connective tissue disorder caused by a mutation of the fibrillin gene and increased TGF-β in tissues. This disorder leads to connective tissue fragility, with such clinical manifestations as slender fingers, long limbs, abnormal cardiac valves, and aortic aneurysm development. We present here a case of Class II maxillary protrusion in a 13-year-old male with MFS. The patient underwent orthodontic treatment, including extractions of the upper and lower bicuspids. The treatment achieved a good Class I occlusion with normal overjet and overbite. On the other hand, we found extraordinary craniofacial skeleton development during the post-adolescent period and untreatable marginal gingivitis despite complete pla...
Background: It is important to establish an early diagnosis of the Marfan Syndrome (MFS) for providi...
Nearly 100 years ago, Antoine Marfan first described a recurrent systemic disorder of connective tis...
Marfan syndrome is caused by mutations in the fibrillin-1 gene (FBN1). The most important features a...
Marfan syndrome is considered a relatively rare genetic disorder that affects the connective tissues...
Marfan syndrome is an autosomal dominant disorder of connective tissue primarily characterized with ...
Marfan syndrome is an autosomal dominant systemic disorder of the connective tissue. Children affect...
Background: Connective tissue disorders, such as some forms of Ehlers-Danlos syndrome, have been ass...
Copyright © 2012 Rajendran Ganesh et al. This is an open access article distributed under the Creati...
Marfan's Syndrome is a multisistemic pathology of connective tissues, a dominant autosomal transmiss...
The Marfan syndrome is an autosomal dominant hereditary connective tissue disorder with variable exp...
Introduction: The role of this study is to highlight a correlation between patients with Marfan synd...
Marfan's syndrome (MFS) is a systemic disorder of connective tissue caused by mutations in the extra...
A síndrome de Marfan é uma doença do tecido conjuntivo, de caráter hereditário, com grande variabili...
Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder. It is caused by a mutatio...
Marfan syndrome (MFS) is an autosomal dominant, age-related but highly penetrant condition with subs...
Background: It is important to establish an early diagnosis of the Marfan Syndrome (MFS) for providi...
Nearly 100 years ago, Antoine Marfan first described a recurrent systemic disorder of connective tis...
Marfan syndrome is caused by mutations in the fibrillin-1 gene (FBN1). The most important features a...
Marfan syndrome is considered a relatively rare genetic disorder that affects the connective tissues...
Marfan syndrome is an autosomal dominant disorder of connective tissue primarily characterized with ...
Marfan syndrome is an autosomal dominant systemic disorder of the connective tissue. Children affect...
Background: Connective tissue disorders, such as some forms of Ehlers-Danlos syndrome, have been ass...
Copyright © 2012 Rajendran Ganesh et al. This is an open access article distributed under the Creati...
Marfan's Syndrome is a multisistemic pathology of connective tissues, a dominant autosomal transmiss...
The Marfan syndrome is an autosomal dominant hereditary connective tissue disorder with variable exp...
Introduction: The role of this study is to highlight a correlation between patients with Marfan synd...
Marfan's syndrome (MFS) is a systemic disorder of connective tissue caused by mutations in the extra...
A síndrome de Marfan é uma doença do tecido conjuntivo, de caráter hereditário, com grande variabili...
Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder. It is caused by a mutatio...
Marfan syndrome (MFS) is an autosomal dominant, age-related but highly penetrant condition with subs...
Background: It is important to establish an early diagnosis of the Marfan Syndrome (MFS) for providi...
Nearly 100 years ago, Antoine Marfan first described a recurrent systemic disorder of connective tis...
Marfan syndrome is caused by mutations in the fibrillin-1 gene (FBN1). The most important features a...