Results 11 to 20 of about 247,154 (290)
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 M. Siismets, Nan E. Hatch
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Clinics in Plastic SurgeryPatients with craniofacial microsomia comprise a diverse clinical cohort that requires individualized attention and surgical consideration that benefits from multidisciplinary team management to optimize functionality and esthetics. Specific concerns regarding airway, vision, feeding, growth, hearing, speech, development, and quality of life may ...
Erin E Anstadt, Craig Birgfeld
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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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The development of the skull of the Egyptian cobra Naja h. haje (Squamata: Serpentes: Elapidae) [PDF]
, 2015 Background: The study of craniofacial development is important in understanding the ontogenetic processes behind morphological diversity. A complete morphological description of the embryonic skull development of the Egyptian cobra, Naja h.
Evans, SE, Khannoon, ER
core +16 more sources
Polymeric Scaffolds for Dental, Oral, and Craniofacial Regenerative Medicine
Molecules, 2021 Dental, oral, and craniofacial (DOC) regenerative medicine aims to repair or regenerate DOC tissues including teeth, dental pulp, periodontal tissues, salivary gland, temporomandibular joint (TMJ), hard (bone, cartilage), and soft (muscle, nerve, skin ...
David T. Wu +6 more
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Haploinsufficiency of SF3B2 causes craniofacial microsomia
Nature Communications, 2021 Craniofacial microsomia (CFM) is the second most common congenital facial anomaly, yet its genetic etiology remains unknown. We perform whole-exome or genome sequencing of 146 kindreds with sporadic (n = 138) or familial (n = 8) CFM, identifying a highly
Andrew T. Timberlake +28 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
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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
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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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