Results 1 to 10 of about 102,054 (167)
Journal of Developmental Biology, 2020 Craniofacial anomalies are among the most common of birth defects. The pathogenesis of craniofacial anomalies frequently involves defects in the migration, proliferation, and fate of neural crest cells destined for the craniofacial skeleton.
Erica Siismets +2 more
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Craniofacial ciliopathies: A new classification for craniofacial disorders [PDF]
American Journal of Medical Genetics, Part A, 2010 AbstractCraniofacial anomalies are some of the most variable and common defects affecting the population. Herein, we examine a group of craniofacial disorders that are the result of defects in primary cilia; ubiquitous, microtubule‐based organelles that transduce molecular signals and facilitate the interactions between the cell and its environment ...
Samantha A Brügmann +2 more
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Journal of Developmental Biology, 2022 The expression of the col11a1a gene is essential for normal skeletal development, affecting both cartilage and bone. Loss of function mutations have been shown to cause abnormalities in the growth plate of long bones, as well as in craniofacial ...
Jonathon C. Reeck, Julia Thom Oxford
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The Skull’s Girder: A Brief Review of the Cranial Base
Journal of Developmental Biology, 2021 The cranial base is a multifunctional bony platform within the core of the cranium, spanning rostral to caudal ends. This structure provides support for the brain and skull vault above, serves as a link between the head and the vertebral column below ...
Shankar Rengasamy Venugopalan +1 more
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Frontiers in Genetics, 2022 Copy number variants (CNVs) associated with neurodevelopmental disorders are characterized by extensive phenotypic heterogeneity. In particular, one CNV was identified in a subset of children clinically diagnosed with intellectual disabilities (ID) that ...
Micaela Lasser +6 more
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Clinics in Plastic Surgery, 2012 Craniofacial microsomia (CFM) is one of the most common congenital conditions treated in craniofacial centers worldwide. This condition is variably associated with anomalies of the jaws, ears, facial soft tissue, orbits, and facial nerve function and can be associated with extracranial anomalies.
Craig, Birgfeld, Carrie, Heike
openaire +3 more sources
Oculo-orbital involvement in craniofacial injuries following road traffic accidents
Indian Journal of Health Sciences and Biomedical Research KLEU, 2021 INTRODUCTION: Craniofacial injury is of common occurrence following road traffic accidents (RTAs). It often leads to serious disabilities, including significant damage to the visual system.
Adyasha Dash, Pradeep Kumar Panigrahi
doaj +1 more source
Coats'-like Response Associated with Linear Scleroderma
Journal of Ophthalmic & Vision Research, 2022 Purpose: To present a case of linear scleroderma known as “en coup de sabre” associated with Coats'- like response. Case Report: A 12-year-old boy presented with subacute painless vision loss in the ipsilateral side of the patient's en coup de sabre ...
Hassan Behboudi +6 more
doaj +1 more source
Determination of Craniofacial Morphometry of Saudi Adults by Steiner’s Analysis [PDF]
Journal of Clinical and Diagnostic Research, 2019 Introduction: Evaluation of craniofacial morphology plays a vital role both in clinical practice and research purpose in dentistry and lateral cephalometric radiograph is the most commonly used and appropriate implement for the evaluation of craniofacial
Ibadullah Kundi +2 more
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Snrpb is required in murine neural crest cells for proper splicing and craniofacial morphogenesis
Disease Models & Mechanisms, 2022 Heterozygous mutations in SNRPB, an essential core component of the five small ribonucleoprotein particles of the spliceosome, are responsible for cerebrocostomandibular syndrome (CCMS).
Sabrina Shameen Alam +10 more
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