The aim of this review is to evaluate the developmental, functional, and morphological aspects of the craniofacial complex in patients with myotonic dystrophy type 1 (DM1), Facioscapulohumeral muscular dystrophy (FSHD), and Duchenne muscular dystrophy (DMD). The degree of disease onset and severity varied from patient to patient, and most parameters indicated a greater degree of deterioration in older patients. It was found that all the muscular dystrophies studied showed altered craniofacial morphology, with malocclusion as the most consistent clinical characteristic. Particularly DM1 patients, who are the most studied, showed significant vertical aberration and post-normal occlusion. DMD patients are reported mainly with altered dental ar...
Contains fulltext : 87385.pdf (publisher's version ) (Closed access)Facioscapulohu...
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) represent the most frequent multisystemic muscular ...
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) represent the most frequent multisystemic muscular ...
Occlusal traits and craniofacial morphology were studied in growing patients with Duchenne muscular ...
The aim of this study was to describe the longitudinal changes in facial morphology, dental arch alt...
SUMMARY Lateral cephalometric radiographs of 35 Japanese male patients suffering from Duchenne muscu...
Myotonic dystrophy type 1 (DM1) is a slowly progressive neuromuscular disease. The overall aim of th...
Copyright © 2002 American Academy of Pediatric DentistryA comprehensive assessment of the dental cha...
PubMed ID: 1891607Fourteen patients suffering from primary muscular disease (myopathies), including ...
Duchenne muscular dystrophy (DMD) affects orofacial function. Our aim was to evaluate certain charac...
A comprehensive assessment of the dental characteristics of 23 patients with Duchenne muscular dystr...
Contains fulltext : 167750.pdf (publisher's version ) (Closed access)Dysphagia in ...
Myotonic dystrophy, or Steinert’s disease, is themost common formofmuscular dystrophy that occurs in...
Objective. the purpose of this stud(y) was to evaluate the masticatory muscles and the temporomandib...
Dysphagia in Duchenne muscular dystrophy (DMD) worsens with age, with increasingly effortful mastica...
Contains fulltext : 87385.pdf (publisher's version ) (Closed access)Facioscapulohu...
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) represent the most frequent multisystemic muscular ...
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) represent the most frequent multisystemic muscular ...
Occlusal traits and craniofacial morphology were studied in growing patients with Duchenne muscular ...
The aim of this study was to describe the longitudinal changes in facial morphology, dental arch alt...
SUMMARY Lateral cephalometric radiographs of 35 Japanese male patients suffering from Duchenne muscu...
Myotonic dystrophy type 1 (DM1) is a slowly progressive neuromuscular disease. The overall aim of th...
Copyright © 2002 American Academy of Pediatric DentistryA comprehensive assessment of the dental cha...
PubMed ID: 1891607Fourteen patients suffering from primary muscular disease (myopathies), including ...
Duchenne muscular dystrophy (DMD) affects orofacial function. Our aim was to evaluate certain charac...
A comprehensive assessment of the dental characteristics of 23 patients with Duchenne muscular dystr...
Contains fulltext : 167750.pdf (publisher's version ) (Closed access)Dysphagia in ...
Myotonic dystrophy, or Steinert’s disease, is themost common formofmuscular dystrophy that occurs in...
Objective. the purpose of this stud(y) was to evaluate the masticatory muscles and the temporomandib...
Dysphagia in Duchenne muscular dystrophy (DMD) worsens with age, with increasingly effortful mastica...
Contains fulltext : 87385.pdf (publisher's version ) (Closed access)Facioscapulohu...
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) represent the most frequent multisystemic muscular ...
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) represent the most frequent multisystemic muscular ...