Results 31 to 40 of about 3,300 (225)
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
Dental implants in patients with oral mucosal alterations : an update [PDF]
Objective: To determine whether a series of diseases of the oral mucosa - Sjögren syndrome, ectodermal dysplasia, epidermolysis bullosa and lichen planus - reduce the survival rate of dental implants. Material and Method: A Medline search was carried out
Ata-Ali Mahmud, Francisco Javier +4 more
core +1 more source
Familial cases of missing mandibular incisor: three case presentations [PDF]
Hypodontia is the congenital absence of one or more teeth because of agenesis. The most commonly missing teeth are the third molars, the maxillary lateral incisors and the second premolars.
Ngeow, Dr. W.C.
core
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
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
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Kepadatan kerang lumpur Anodontia edentula Linnaeus, 1758 kaitannya dengan parameter lingkungan di Kabupaten Muna [PDF]
The research aims to analyze the density of mud clams Anodintia edentula Linnaeus, 1758 relation to environmental parameters, covering organic material content and composition of sediment in Muna regency. Research carried out in coastal Lambiku and Tobea
Omar, Sharifuddin Bin Andy +2 more
core
Effect of hairless gene polymorphism on the breeding values of milk production traits in Valle del Belice sheep [PDF]
The aim of this work was to assess the association between the hairless genotypes and estimated breeding values (EBVs) for milk yield (MY), fat (FAT) and protein (PRT) content in Valle del Belice dairy sheep breed.
MASTRANGELO, Salvatore +3 more
core +1 more source

