Results 231 to 240 of about 78,021 (259)

Multiple Supernumeraries in a Non-Syndromic Patient

Journal of Clinical Pediatric Dentistry, 2012
Presence of supernumerary teeth (ST) in non-syndromic patients is an exceptional event. The aim of this article is to present an unusual case of a non-syndromic 12 years old girl with 12 ST. In the reported case supernumeraries were found in three quadrants and the most common ST were bicuspids.
Ledesma-Montes C, Garcés-Ortíz, Juan Francisco, Salcido-García, Florentino, Hernández-Flores, Maricela, Garcés-Ortíz   +3 more
openaire   +2 more sources

Non-syndromic oxycephaly and brachycephaly: a review

Child's Nervous System, 2012
Non-syndromic coronal synostoses oxycephaly and brachycephaly (NSCSOB) are rare. Their natural history, surgical management, and outcome are debated.We reviewed the available literature on NSCSOB. In addition, we reviewed retrospectively our experience with cases of NSCSOB, managed and operated by our joint craniofacial team since 1984.
Matthieu, Vinchon, Philippe, Pellerin, Marc, Baroncini, Alexis, Wolber, Patrick, Dhellemmes   +4 more
openaire   +2 more sources

Retinitis Pigmentosa (Non-syndromic)

The PDE complex has one α, one β, and two γ subunits. Mutations in each subunit can lead to AR-RP. The complex encodes a protein that play an important role in rod phototransduction and maintenance of the intracellular cGMP level by activating cGMP in response to photons.
Ahmet, Hondur, Stephen, Tsang, Tarun, Sharma, Vlad, Diaconita   +3 more
openaire   +2 more sources

Cloning Genes for Non-Syndromal Hearing Impairment

British Journal of Audiology, 1999
Over 45 genes that cause autosomal non-syndromic hearing impairment (NSHI) have been localized and many more are predicted to exist. To clone these genes, a number of different strategies can be used. This paper focuses on four general approaches: functional cloning, positional cloning, position-dependent candidate gene cloning, and position ...
Smith, R.J.H., Van Camp, G.
openaire   +3 more sources

[Non syndromic craniosynostosis].

Annales de chirurgie plastique et esthetique, 2017
Craniosynostosis are rare congenital malformations of the skull resulting from the premature fusion of one or several cranial sutures. Prevalence is considered in approximately 1 on 2000 births. Non syndromic craniosynostosis (NSC) or isolated form are the most frequent forms (85 % of the cases).
Y, Bennis, A, Wolber, M, Vinchon, A, Belkhou, V, Duquennoy-Martinot, P, Guerreschi   +5 more
openaire   +1 more source

Syndromic Hydrocephalus

Neurosurgery Clinics of North America, 2022
Jennifer M Strahle, Sai Anusha Sanka
exaly  

Non-Syndromic Dominant DFNA1

2000
E D, Lynch, P E, León
openaire   +2 more sources

Panels and Syndromic Testing in Clinical Microbiology

Clinics in Laboratory Medicine, 2020
Jennifer Dien Bard, Erin McElvania
exaly  

Genetic and epigenetic studies in non-syndromic oral clefts

Oral Diseases, 2022
Azeez A Alade, Azeez Butali, Waheed Awotoye   +2 more
exaly  

Syndromic and non‐syndromic GLI3 phenotypes

Clinical Genetics, 2005
L G, Biesecker, J, Johnston
openaire   +2 more sources