AI Article Synopsis

  • TAR syndrome is a congenital condition characterized by low platelet counts and underdevelopment or absence of radial bones, often leading to associated health issues like cardiac and gastrointestinal anomalies.
  • It can increase the risk of dental and craniofacial trauma, making it crucial for dental professionals to understand the syndrome for effective patient care.
  • A case study of a 26-year-old patient illustrates the successful management of dental trauma and root fracture using advanced surgical techniques and a collaborative approach with a hematologist throughout the treatment.

Article Abstract

Thrombocytopenia-absent radius (TAR) syndrome is a congenital malformation in which affected individuals present reductions in the number of platelets, hypoplasia, or absence of radial bone unilaterally or bilaterally. Hematologic, skeletal, cardiac (particularly tetralogy of Fallot and septal-atrial defects), and gastrointestinal anomalies are most commonly associated with TAR syndrome. Skeletal changes result in a higher risk of dental and craniofacial trauma in patients with the syndrome. Thus, it is important for the dentist to be aware of the characteristics of TAR syndrome and its clinical management for better care of these patients. The objective of this study is to describe a case report of a 26-year-old patient with TAR syndrome with a history of trauma and root fracture of tooth 11 and alveolar bone ridge. During anamnesis, root fractures requiring the extraction of the 11 tooth, alveolar bone ridge fracture in the adjacent region, and dental trauma were observed. A hematological evaluation and blood and radiological examinations were performed. Osseointegrated implant was performed using the guided surgery and flapless technique, as well as prosthetic rehabilitation in the affected region. This report discusses the importance of careful planning, such as the use of incisions and conservative surgery, techniques for alveolar ridge preservation, gingival manipulation, and prosthesis confection. The patient was attended by a hematologist throughout the treatment. TAR syndrome, absent radii and thrombocytopenia, dental implants, oral surgery.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700778PMC
http://dx.doi.org/10.4317/jced.56642DOI Listing

Publication Analysis

Top Keywords

tar syndrome
20
thrombocytopenia-absent radius
8
radius tar
8
case report
8
tooth alveolar
8
alveolar bone
8
bone ridge
8
tar
6
syndrome
6
tar case
4

Similar Publications

An Algorithm for Management of Radial Longitudinal Deficiency.

J Hand Surg Asian Pac Vol

December 2024

Department of Hand Surgery, Kasturba Medical College Manipal, Manipal Academy Of Higher Education, Manipal, Karnataka, India.

Article Synopsis
  • - The management of radial longitudinal deficiency (RLD) lacks specific guidelines, resulting in varied treatment approaches that complicate the determination of effective interventions for individual patients.
  • - Approximately 40% of RLD cases are associated with syndromes like Holt-Oram, TAR, and VACTERL, making it essential for hand surgeons to recognize these conditions and their implications for treatment.
  • - Surgical procedures like centralisation and radialisation are fundamental for treatment, but current methods do not fully restore normal wrist function; emerging techniques focus on improving biomechanics and considering proximal limb changes in management.
View Article and Find Full Text PDF

Purpose: Classification systems and treatment for children with radial longitudinal deficiency are classically focused on the hand and wrist. However, the elbow can affect the function of these patients secondary to stiffness or instability. The objective of this study was to determine if a correlation exists between severity of radial longitudinal deficiency (RLD) and degree of proximal ulnar hypoplasia.

View Article and Find Full Text PDF

The co-occurrence of Thrombocytopenia with Absent Radius (TAR) syndrome and Langerhans Cell Histiocytosis (LCH) is exceedingly rare, with scant documentation in existing medical literature. This case report aims to shed light on this unique intersection of conditions, emphasizing the diagnostic and therapeutic challenges it presents. A 27-year-old female with a history of TAR syndrome presented with microcytic anemia, hip pain, and gastrointestinal symptoms.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!