Results 91 to 100 of about 4,054 (202)
Restorative Management of Dentinogenesis Imperfecta in an adult - A case report
Nigerian Dental Journal, 2020 Dentinogenesis Imperfecta is a localized mesodermal dysplasia affecting both the primary and permanent dentition. First described in the late 19th century, it is characterized by discolored and translucent teeth ranging from grey to brownish-blue or ...
A.O. Awotile, L.L. Enone, A. Oyapero
doaj +1 more source
Clinical and Experimental Dental Research, Volume 10, Issue 4, August 2024.ABSTRACT Objectives To evaluate the validity of the Golden Proportion, Golden Percentage, and Recurring Esthetic Dental (RED) Proportion among Kenyans of African descent with naturally well‐aligned teeth. Materials and Methods Standardized frontal photographic images of the smiles of 175 participants aged 18–35 years were obtained, and Adobe Photoshop ...
Marion N. Mosomi +3 more
wiley +1 more source
A Single Recurrent Mutation in the 5′-UTR of IFITM5 Causes Osteogenesis Imperfecta Type V [PDF]
, 2012 Osteogenesis imperfecta (OI) is a heterogenous group of genetic disorders of bone fragility. OI type V is an autosomal-dominant disease characterized by calcification of the forearm interosseous membrane, radial head dislocation, a subphyseal metaphyseal
Cho, Tae-Joon +18 more
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Genotype and phenotype in patients with ACAN gene variants: Three cases and literature review
Molecular Genetics &Genomic Medicine, Volume 12, Issue 4, April 2024.No clear genotype–phenotype relationship of patients with ACAN variants were found. Gene sequencing is necessary to diagnose ACAN variant caused short stature. In general, appropriate rhGH and/or GnRHa therapy can improve the adult height of affected pediatric patients caused by ACAN variants.
Wei Tang +6 more
wiley +1 more source
Dental tissue changes in juvenile and adult mice with osteogenesis imperfecta
The Anatomical Record, Volume 307, Issue 3, Page 600-610, March 2024.Abstract Osteogenesis imperfecta (OI), a disorder of type I collagen, causes skeletal deformities as well as defects in dental tissues, which lead to increased enamel wear and smaller teeth with shorter roots. Mice with OI exhibit similar microstructural dentin changes, including reduced dentin tubule density and dentin cross‐sectional area.
Jacob C. Moore +7 more
wiley +1 more source
Saudi Dental Journal, 2013 Dentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic disorder that affects the connective tissues and results in dentine dysplasia.
Halima Abukabbos, Faisal Al-Sineedi
doaj
Swellings over the Limbs as the Earliest Feature in a Patient with Osteogenesis Imperfecta Type V
Case Reports in Orthopedics, 2014 Swellings over the upper and lower limbs were encountered in a one-year-old child. Skeletal survey showed a constellation of distinctive radiographic abnormalities of osteoporosis, hyperplastic callus and ossification of the interosseous membrane of the ...
Ali Al Kaissi +3 more
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Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review
Acta Dermato-Venereologica, 2020 Ehlers-Danlos syndromes (EDS) are a group of inherited connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and variable tissue fragility. However, there are limited published data on the dental manifestations of EDS.
Ines Kapferer-Seebacher +3 more
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Molar‐incisor‐malformation in a paediatric cancer patient: Case report
Oral Surgery, Volume 17, Issue 1, Page 53-58, February 2024.Abstract Aim To report a case of molar‐incisor‐malformation (MIM) in a 7‐year‐old boy with a history of congenital infantile fibrosarcoma of the upper chest, which was surgically treated, without adjuvant radio/chemotherapy. Material and Methods The boy presented with mobility and pain on percussion of the permanent mandibular first molars.
Athina Tosiou +4 more
wiley +1 more source
Intrafibrillar Mineral May be Absent in Dentinogenesis Imperfecta Type II (DI-II) [PDF]
, 2001 J.H. Kinney +5 more
openalex +3 more sources