The mouth, located in the lower third of the face, is a uniquely visible structure. It serves as a
vital organ both aesthetically and functionally, playing a key role in speech, expression, and …

Statement of problem: Prosthetic techniques commonly employed for the rehabilitation of
edentulous patients might not be adequate in the treatment of patients with microstomia …

The problem of small oral aperture is big. Irrespective of the etiology, this problem may be
overcome by adjunctive therapies in the form of prosthesis, surgery, or exercise. A patient is …

ABSTRACT Background Freeman-Sheldon syndrome is a rare hereditary disorder
characterised by three basic abnormalities, namely microstomia, camptodactyly with ulnar …

We report a case of a male baby who has characteristic signs of Freeman–Sheldon
syndrome, a rare but recognizable, severe autosomal dominant form of distal arthrogryposis …

In the context of a case presentation of a 16-year-old girl treated for retrognathia associated
with Freeman-Burian syndrome (FBS), importance of early orthodontic evaluation and …

Introducción: el síndrome de Freeman-Sheldon (SFS), es un trastorno genético
caracterizado por un estado dismórfico, incluyendo manifestaciones tales como: anomalías …

El síndrome de Freeman Sheldon (SFS), descrito como parte del grupo de artrogriposis
distales, se caracteriza por anomalías óseas y contracturas articulares con facies …

We report a case of a male baby who has characteristic signs of Freeman–Sheldon
syndrome, a rare but recognizable, severe autosomal dominant form of distal arthrogryposis …

Entre sus características clínicas se pueden llegar a encontrar: en cara: hipoplasia de la
región media de la cara, filtro alargado, pliegues nasolabiales, hipertelorismo, estrabismo …