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Frontiers in Psychology, 2023 IntroductionThe higher rate of neuropsychiatric disorders in individuals with non-syndromic orofacial clefts has been well documented by previous studies. Our goal was to identify children with non-syndromic orofacial clefts that are at risk for abnormal
Kinga Amália Sándor-Bajusz +7 more
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Non-syndromic hereditary gingival fibromatosis [PDF]
BMJ Case Reports, 2013 Hereditary gingival fibromatosis is a rare condition characterised by severe gingival hyperplasia that can occur as an isolated disease or as part of a syndrome or chromosomal abnormality. In severe cases, the gingival enlargement may cover the crowns of teeth and cause severe aesthetic, emotional and functional impairment.
Ravi Prakash Sasankoti, Mohan +3 more
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Post-operative neurodevelopmental findings in syndromic and non-syndromic craniosynostosis [PDF]
, 2010 Objective To evaluate the developmental situation of children that undergo operation because of syndromic and non-syndromic craniosynostosis.
Enayatollah, A.N. +3 more
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Non Syndromic Familial Bilateral Decidious Taurodontism – A First Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2014 Taurodontism is anatomical and morphological alteration in the shape of the tooth. In taurodontism the crowns appear larger and the roots shorter compared to the normal anatomy of the respective tooth.
ANTARMAYEE PANIGRAHI +4 more
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Genetic Variants in miRNAs Are Associated With Risk of Non-syndromic Tooth Agenesis
Frontiers in Physiology, 2020 Non-syndromic tooth agenesis (NSTA) is one of the most common dental abnormalities. MiRNAs participated in the craniofacial and tooth development. Therefore, single nucleotide polymorphisms (SNPs) in miRNA genes may contribute to the susceptibility of ...
Min Gu +19 more
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Rare non‐syndromic bilateral maxillary and mandibular permanent canine agenesis
Clinical Case Reports, 2022 Oligodontia or absence of teeth such as the Canines is rare and is often accompanied with several other missing teeth. This condition may also be accompanied with morphological and growth related changes in the teeth and the maxillofacial complex ...
Anand Marya +2 more
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Molecular genetics of non-syndromic deafness
Brazilian Journal of Otorhinolaryngology, 2005 One in every 1,000 newborn suffers from congenital hearing impairment. More than 60% of the congenital cases are caused by genetic factors. In most cases, hearing loss is a multifactorial disorder caused by both genetic and environmental factors. Molecular genetics of deafness has experienced remarkable progress in the last decade.
Piatto, Vânia B. +6 more
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Genetics of non syndromic hearing loss [PDF]
Medical Journal Armed Forces India, 2015 Non Syndromic Hearing Loss is an important cause for hearing loss. One in 1000 newborns have some hearing impairment. Over 400 genetic syndromes have been described. Non Syndromic Hearing Loss (NSHL) can be inherited in an Autosomal Dominant, Autosomal Recessive or a Sex Linked fashion.
M D, Venkatesh +2 more
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NON SYNDROMIC BILATERAL CONGENITAL LIP PITS: A CASE REPORT [PDF]
, 2014 Lip pits are a rare developmental entity that affects the region of upper and lower lips or the commissure of the lips. Most often the condition is associated with syndromes constituting other features apart from lip pits.
Moidin Shakil +3 more
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Non syndromic supernumerary teeth: management of two clinical cases
The Pan African Medical Journal, 2018 Supernumerary teeth are extra teeth or tooth-like structures. Single, double, or multiple teeth that occur in one or both jaws may be erupted or unerupted and unilateral or bilateral. Supernumeraries are less common in primary dentition than in permanent
Akram Belmehdi +3 more
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