Results 31 to 40 of about 3,257 (209)
Sanjad-Sakati Syndrome Dental Management: A Case Report [PDF]
, 2013 Sanjad-Sakati syndrome (SSS) is a rare genetic disorder with autosomal recessive pattern of inheritance characterized by hypoparathyroidism, sever growth failure, mental retardation, susceptibility to chest infection, and dentofacial anomalies.
Hisham Y. El Batawi
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Prosthetic rehabilitation of a young patient with Hypophosphatasia - A review and case report
Contemporary Clinical Dentistry, 2012 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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Effect of hairless gene polymorphism on the breeding values of milk production traits in Valle del Belice sheep [PDF]
, 2013 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
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Dental implants in patients with oral mucosal alterations : an update [PDF]
, 2011 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
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Recreating the missing smile: A case report on ectodermal dysplasia
SRM Journal of Research in Dental Sciences, 2012 Ectodermal dysplasia syndrome is a group of hereditary disorders affecting the structures developing from the ectoderm. More than 150 different types have been described with the most common being the hypohidrotic and the hidrotic types.
R Shakila +3 more
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Checklist of the Invertebrate Animals Reported from the Region of Port Aransas, Texas [PDF]
, 1960 This checklist is of preliminary form with the hope that this will be a beginning for a more complete annotated list of the fauna and flora of this region. In many cases this list is quite obviously incomplete, however further work on the taxonomy of
Trott, Lamarr B.
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Revista da Faculdade de Odontologia de Porto Alegre, 2009 The objective of the present article is to report an uncommon case of a boy with history of 11 natal lost teeth, all belonging to the normal series of primary dentition, associated with absence of up to 21 permanent tooth germs. Such a condition resulted
Patricia Fernanda Dias +3 more
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The Incidence of Tooth Agenesis in Pediatric Patients in the Olomouc Region
Česká Stomatologie a Praktické Zubní Lékařství, 2014 Aim of the study: Many developmental anomalies can occur in craniofacial region. Dental developmental anomalies, namely hypodontia, are the most often of them.
L. Kramerová +3 more
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Familial cases of missing mandibular incisor: three case presentations [PDF]
, 1999 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.
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American Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 790-799, April 2026.ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani +17 more
wiley +1 more source