Results 11 to 20 of about 78,021 (259)
Familial non-syndromic oligodontia
Journal of Indian Academy of Oral Medicine and Radiology, 2015 Oligodontia, a rare genetic disorder, represents the congenital absence of more than six teeth in primary, permanent, or both dentitions and is usually the feature of a syndrome. Its occurrence as an isolated entity is even rarer.
Seema Basoya +3 more
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Non-syndromic supernumerary premolars [PDF]
Medicina Oral Patología Oral y Cirugia Bucal, 2011 Objective: The objective of this study was to estimate the incidence of non-syndromic supernumerary premolars, to classify them and to identify the complications related to them. Study Design: This retrospective cohort study was composed of 8400 panoramic radiographs of patients who presented at our Oral and Maxillofacial Surgery Services from January ...
YAPıCı, G +3 more
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Non-syndromic retinitis pigmentosa [PDF]
Progress in Retinal and Eye Research, 2018 Retinitis pigmentosa (RP) encompasses a group of inherited retinal dystrophies characterized by the primary degeneration of rod and cone photoreceptors. RP is a leading cause of visual disability, with a worldwide prevalence of 1:4000. Although the majority of RP cases are non-syndromic, 20-30% of patients with RP also have an associated non-ocular ...
Verbakel, S.K. +9 more
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Non-syndromic double lip [PDF]
BMJ Case Reports, 2013 A 57-year-old man reported to the outpatient department with the chief compliant of deformed upper lip which was present since birth. He denied any complaints other than cosmetic ones. On examination, an extra fold of redundant tissue was present on the inner surface of the upper lip. The …
Ravi Prakash Sasankoti, Mohan +3 more
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Non-Syndromal Facial Asymmetry [PDF]
Medical Journal Armed Forces India, 2005 Absolute facial symmetry of the two halves of the face is of very rare occurrence and some degree of right/left variation is not an exception but a rule. Although each person shares with the rest of the population, many characteristics, there are enough differences to make each human being a unique individual.
G K, Thapliyal +2 more
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Genetic insights into non-syndromic Tetralogy of Fallot
Frontiers in Physiology, 2022 Congenital heart defects (CHD) include structural abnormalities of the heart or/and great vessels that are present at birth. CHD affects around 1% of all newborns worldwide.
Nouf J. Althali +2 more
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Global Medical Genetics, 2022 Non-syndromic cleft lip and palate (NSCLP) is one of the most common birth defects in humans with an overall prevalence of ∼1 in 700 live births around the world.
Mahamad Irfanulla Khan +2 more
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Recent advances in genetic etiology of non-syndromic deafness in children
Frontiers in Neuroscience, 2023 Congenital auditory impairment is a prevalent anomaly observed in approximately 2–3 per 1,000 infants. The consequences associated with hearing loss among children encompass the decline of verbal communication, linguistic skills, educational progress ...
Yawei Feng +3 more
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Supernumerary teeth in non-syndromic patients [PDF]
Imaging Science in Dentistry, 2012 Hyperdontia or supernumerary teeth without associated syndrome is a rare phenomenon, as supernumerary teeth are usually associated with cleft lip and palate or other syndromes such as Gardner's syndrome, cleidocranial dysplasia, and so on. Five patients with supernumerary teeth visited our department.
Mali, Santosh +3 more
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Journal of Pediatric Neurosciences, 2020 Aims and Objectives: This study aimed to analyze the spectrum and surgical outcome of cases of craniosynostosis operated at a tertiary referral institute in IndiaDesign: This was a cross-sectional study. Materials and Methods: We retrospectively examined
Charandeep S Gandhoke +4 more
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