Results 21 to 30 of about 1,605 (178)
Step Wise Management of Asyndromic Tooth Agenesis with Ankyloglossia: A Case Report [PDF]
Ankyloglossia or tongue tie refers to restricted tongue movements, diagnosed in early childhood and adolescence that may cause changes in bone growth and other orofacial tissues results in altered oral functions of the child.
Vandana R Gadve, Vijaya S Dhote
doaj +1 more source
Primary Teeth Supported Fixed Prosthesis—A Predictable Treatment Alternative
Background: Individuals with tooth agenesis often present a significant clinical challenge for dental practitioners. This retrospective study evaluated clinical and radiological long-term functional and esthetic outcomes following restoration using ...
Sarit Naishlos +8 more
doaj +1 more source
Prosthodontic management of anhidrotic ectodermal dysplasia
Ectodermal dysplasia is characterized by the absence or defects of two or more ectodermally derived structures. Anodontia or hypodontia is the most striking dental manifestation. In severe hypodontia, there is lack of alveolar development with consequent
Shilpy Gupta, Parimala Tyagi
doaj +1 more source
Early prosthodontic intervention in a child patient of hypohidrotic ectodermal dysplasia
The ectodermal dysplasias (EDs) comprise a large, heterogeneous group of inherited disorders that are defined by primary defects in the development of two or more tissues derived from embryonic ectoderm.
Culatur Thulasingam +2 more
doaj +1 more source
Implants have gained tremendous popularity as a treatment modality for replacement of missing teeth in adults. There is extensive research present on the use of implants in adults, but there is a dearth of data available on the same in adolescents.
Rohit A Shah +5 more
doaj +1 more source
Solitary median maxillary central incisor (SMMCI) is a rare dental anomaly. It is estimated to occur in 1:50,000 live births. The SMMCI tooth differs from the normal central incisor in that the crown form is symmetric and it develops and erupts precisely
Ashok Utreja +2 more
doaj +1 more source
X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle
Ectodermal dysplasias are a large group of rare genetic disorders characterized by impaired development of hair, teeth, and eccrine glands in humans, mice, and cattle.
Drögemüller Cord +2 more
doaj +1 more source
Prosthetic rehabilitation of a young patient with Hypophosphatasia - A review and case report
Hypophosphatasia is a congenital disease characterized by deficiency of serum and tissue non-specific alkaline phosphatase activity. The disease occurs due to mutations in the liver/bone/kidney alkaline phosphatase gene.
Partapjot S Grewal, Kanu Priya Gupta
doaj +1 more source
This review reveals major genetic data gaps for Philippine mangrove fauna, especially invertebrates, limiting species‐level eDNA detection. By compiling 48 years of biodiversity records and assessing reference library coverage, it highlights the need for targeted sequencing and shows how integrating eDNA with conventional surveys strengthens monitoring
Earl Kevin T. Cooper +14 more
wiley +1 more source
Treatment of pediatric patients with partial anodontia is a challenge requiring interdisciplinary approach. Growth period, reduced vertical dimension, microdontia, and unacceptable esthetics present difficulties at various stages of prosthetic ...
Natarajan Kalavathy +4 more
doaj +1 more source

