Introduction. Rubinstein-Taybi syndrome (RTS) is a rare disorder affecting I of 300,000 people, characterized by growth, mental and motor retardation, small stature, broad thumbs and toes, characteristic face, high-arched palate, and recurrent respiratory infections.Case report. the present report describes the periodontal and immunological status of a 14-year-old female patient with RTS. Probing depth, clinical attachment level, bleeding on probing, and radiographic evaluation were performed. Periodontal examination revealed severe attachment loss in incisors and molars and generalized bleeding on probing. Periodontal treatment consisted of scaling and root planing and oral hygiene instructions. Periodontal treatment resulted in resolution...
BackgroundRubinstein-Taybi syndrome (RSTS) is an extremely rare autosomal dominant genetic disease, ...
Rubinstein-Taybi syndrome (RSTS) is an autosomal dominant disorder, caused by loss-of-function varia...
Introduction: Papillon-Lefèvre syndrome is a rare autosomal recessive disorder. This syndrome is cha...
Rubinstein-Taybi syndrome or Broad Thumb-Hallux syndrome is a genetic disorder characterized by faci...
Introduction: Oral and dental (OD) disorders in children with Rubinstein-Taybi syndrome (RTS) are fr...
Oral findings in 45 patients with Rubinstein-Taybi syndrome living in The Netherlands are compared w...
Rubinstein-Taybi syndrome (RSTS) is an uncommon genetic disorder characterised by a typical facies, ...
ABSTRACTMedical and dental care for special needs patients oftentimes require effective and rapid cl...
Rubinstein-Taybi syndrome is a rare genetic multisystem disorder characterized by typical facial dim...
A Síndrome de Rubinstein-Taybi foi primeiramente descrita em 1963 pelos médicos Jack Rubinstein & Ho...
In adolescents periodontal destruction may be the primary manifestation of an as yet unrecognized ra...
Background: Connective tissue disorders, such as some forms of Ehlers-Danlos syndrome, have been ass...
Background: Plasminogen deficiency is a rare autosomal recessive disease, which is associated with a...
BACKGROUND: Plasminogen deficiency is a rare autosomal recessive disease, which is associated with a...
Background: Zimmermann-Laband syndrome is a rare autosomal dominant disorder that is characterized b...
BackgroundRubinstein-Taybi syndrome (RSTS) is an extremely rare autosomal dominant genetic disease, ...
Rubinstein-Taybi syndrome (RSTS) is an autosomal dominant disorder, caused by loss-of-function varia...
Introduction: Papillon-Lefèvre syndrome is a rare autosomal recessive disorder. This syndrome is cha...
Rubinstein-Taybi syndrome or Broad Thumb-Hallux syndrome is a genetic disorder characterized by faci...
Introduction: Oral and dental (OD) disorders in children with Rubinstein-Taybi syndrome (RTS) are fr...
Oral findings in 45 patients with Rubinstein-Taybi syndrome living in The Netherlands are compared w...
Rubinstein-Taybi syndrome (RSTS) is an uncommon genetic disorder characterised by a typical facies, ...
ABSTRACTMedical and dental care for special needs patients oftentimes require effective and rapid cl...
Rubinstein-Taybi syndrome is a rare genetic multisystem disorder characterized by typical facial dim...
A Síndrome de Rubinstein-Taybi foi primeiramente descrita em 1963 pelos médicos Jack Rubinstein & Ho...
In adolescents periodontal destruction may be the primary manifestation of an as yet unrecognized ra...
Background: Connective tissue disorders, such as some forms of Ehlers-Danlos syndrome, have been ass...
Background: Plasminogen deficiency is a rare autosomal recessive disease, which is associated with a...
BACKGROUND: Plasminogen deficiency is a rare autosomal recessive disease, which is associated with a...
Background: Zimmermann-Laband syndrome is a rare autosomal dominant disorder that is characterized b...
BackgroundRubinstein-Taybi syndrome (RSTS) is an extremely rare autosomal dominant genetic disease, ...
Rubinstein-Taybi syndrome (RSTS) is an autosomal dominant disorder, caused by loss-of-function varia...
Introduction: Papillon-Lefèvre syndrome is a rare autosomal recessive disorder. This syndrome is cha...