Showing 301 - 320 results of 323 for search '"craniofacial"', query time: 0.05s Refine Results
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    Zellweger syndrome; identification of mutations in PEX19 and PEX26 gene in Saudi families by Abdulfatah M. Alayoubi, Ambreen Ijaz, Abdul Wali, Jamil A. Hashmi, Azizah Alharbi, Sulman Basit

    Published 2025-12-01
    “…It is characterized by neurological dysfunction, hypotonia, ocular anomalies, craniofacial abnormalities, and absence of peroxisomes in fibroblasts. …”
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    Tracheostomy in temporomandibular joint ankylosis – A review of the literature and case report by Marshall F. Newman, Elizabeth Floodeen, Zachary Gardner

    Published 2025-03-01
    “…A variety of literature is available for patients with craniofacial anomalies who may require tracheostomy and who may develop TMJ ankylosis from a young age, but no literature is available to provide evidenced-based treatment guidelines for adult patients with ankylosis who may be at increased risk for airway compromise. …”
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    Women Are More Susceptible to Caries but Individuals Born with Clefts Are Not by Aditi Jindal, Michelle McMeans, Somnya Narayanan, Erin K. Rose, Shilpa Jain, Mary L. Marazita, Renato Menezes, Ariadne Letra, Flavia M. Carvalho, Carla A. Brandon, Judith M. Resick, Juan C. Mereb, Fernando A. Poletta, Jorge S. Lopez-Camelo, Eduardo E. Castilla, Iêda M. Orioli, Alexandre R. Vieira

    Published 2011-01-01
    “…Isolated forms of cleft lip and palate are among the most common craniofacial congenital anomalies in humans. Historically, several reports suggest that individuals born with clefts have a higher risk for caries. …”
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    Identification and functional analysis of a novel SMARCC2 splicing variant in a family with syndromic neurodevelopmental disorder by Ming Li, Jingqi Lin, Hongjun Fei, Jinyu Liu, Yiyao Chen, Xu Han, Yanlin Wang, Jian Wang, Renyi Hua, Shuyuan Li, Niu Li

    Published 2025-02-01
    “…Results The twin adult males displayed comparable phenotypes, characterized by moderate developmental delay, intellectual and language delays, dense hair, craniofacial anomalies, scoliosis, cryptorchidism, hypotonia, behavioral abnormalities, allergic purpura and eczema, and drug allergies. …”
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