Showing 761 - 780 results of 1,106 for search '"Boys ', query time: 0.07s Refine Results
  1. 761

    Effective and Efficient Correction of Severe Skeletal Class II Division 1 Malocclusion with Intermaxillary Elastics by Mohammed K. Badri

    Published 2021-01-01
    “…This case report describes a successful management of a 12-year-old young adolescent boy that was presented with a Class II division 1 malocclusion with an underlying skeletal discrepancy in horizontal and vertical dimensions. …”
    Get full text
    Article
  2. 762

    Microduplication of 3p26.3 Implicated in Cognitive Development by Leah Te Weehi, Raj Maikoo, Adrian Mc Cormack, Roberto Mazzaschi, Fern Ashton, Liangtao Zhang, Alice M. George, Donald R. Love

    Published 2014-01-01
    “…We report here a 34-month-old boy with global developmental delay referred for molecular karyotyping and fragile X studies. …”
    Get full text
    Article
  3. 763

    Pseudoaneurysm of the Common Carotid Artery in an Infant due to Swallowed Fish Bone by Moulion Tapouh Jean Roger, Fokou Marcus, Fongang Emmanuel, Moifo Boniface, Juimo Alain Georges

    Published 2015-01-01
    “…This paper reports the case of a giant pseudoaneurysm of the left common carotid artery due to swallowed fish bone by an 8-year-old boy. This pseudoaneurysm was 5.5 cm transverse-diameter and resulted in severe respiratory distress. …”
    Get full text
    Article
  4. 764

    Dziecko w ramach wojny. Przypadek Donbasu by Wojciech Siegień

    Published 2021-09-01
    “…Based on the analysis of materials from the Russian media (the case of crucifixion of a boy in Slavyansk) and ethnographic interviews with teachers in Kramatorsk, the author asks questions about the mechanisms of constructing the ontologies of child subjects by institutions of power in the conditions of war and the differentiation of grief after them. …”
    Get full text
    Article
  5. 765

    Acquired Umbilico-Inguinal Fistula with Persistent Discharge due to Suture Reaction: A Case Report and Review of the Literature by Muazez Cevik

    Published 2012-01-01
    “…The aim of this paper is to stay a very rare umbilico-inguinal fistula (UIF) resulting from a delayed suture reaction after the use of silk suture to repair an inguinal hernia. A 3-year-old boy presented with persistent umbilical discharge. …”
    Get full text
    Article
  6. 766
  7. 767
  8. 768

    Bladder Wall Telangiectasia in a Patient with Ataxia-Telangiectasia and How to Manage? by Fatma Deniz Aygün, Serdar Nepesov, Haluk Çokuğraş, Yıldız Camcıoğlu

    Published 2015-01-01
    “…We aimed to report recurrent hemorrhage from bladder wall telangiectasia in a 9-year-old boy with A-T who had received intravenous cyclophosphamide for non-Hodgkin’s lymphoma. …”
    Get full text
    Article
  9. 769

    Symphysis Pubis Osteomyelitis with Bilateral Adductor Muscles Abscess by Saad M. Alqahtani, Fan Jiang, Bardia Barimani, Marie Gdalevitch

    Published 2014-01-01
    “…We present a case that to our knowledge is the first case in literature of osteomyelitis of the pubic symphysis in a 17-year-old boy with juvenile idiopathic arthritis (JIA), which was initially misdiagnosed and progressed to bilateral adductor abscesses. …”
    Get full text
    Article
  10. 770

    Prosthodontic Rehabilitation of Hereditary Ectodermal Dysplasia in an 11-Year-Old Patient with Flexible Denture: A Case Report by Neha Jain, Dinesh Naitam, Arti Wadkar, Anuradha Nemane, Shiva Katoch, Ashish Dewangan

    Published 2012-01-01
    “…This clinical report describes the prosthetic rehabilitation of an 11-year-old boy with hereditary ectodermal dysplasia. Maxillary flexible removable partial denture and mandibular conventional complete denture were fabricated to establish an acceptable masticatory function, speech, and esthetics for the patient.…”
    Get full text
    Article
  11. 771

    Case Report of Nonfamilial Cherubism in a Toddler: Description of Clinic-Radiographic Features and Osseous-Dental Treatments by Mitra Karbasi Kheir

    Published 2016-01-01
    “…Most of the cherubism cases show familial history, but there are some cases without familial histories of disorder. A two-year-old boy with a painless symmetrical progressive swelling of the jaws had visited maxillofacial radiology department. …”
    Get full text
    Article
  12. 772

    Erythema Multiforme Attributable to Herpes Simplex Virus: Clinical Aspects and Treatment by Aya Mtiri, Ghada Bouslama, Nour-sayda Ben Messouad, Iyadh Abidi, Souha Ben Youssef, Badreddine Sriha

    Published 2021-01-01
    “…We report a case of recurrent herpes-associated erythema multiforme managed with prophylactic acyclovir for 6 months: a 17-year-old boy had recurrent cutaneous lesions as well as lesions in the oral cavity and lips. …”
    Get full text
    Article
  13. 773

    The Masquerades of a Childhood Ciliary Body Medulloepithelioma: A Case of Chronic Uveitis, Cataract, and Secondary Glaucoma by Jocelyn Chua, Wisam J. Muen, Ashwin Reddy, John Brookes

    Published 2012-01-01
    “…We report a case where a ciliary body medulloepithelioma in a two-year-old boy presents with chronic uveitis, cataract, and an uncontrolled secondary glaucoma after an innocuous blunt ocular trauma. …”
    Get full text
    Article
  14. 774

    Early Bifrontal Brain Injury: Disturbances in Cognitive Function Development by Christine Bonnier, Aurélie Costet, Ghassan Hmaimess, Corinne Catale, Christelle Maillart, Patricia Marique

    Published 2010-01-01
    “…We describe six psychomotor, language, and neuropsychological sequential developmental evaluations in a boy who sustained a severe bifrontal traumatic brain injury (TBI) at 19 months of age. …”
    Get full text
    Article
  15. 775

    Hair Coil Penile Tourniquet Syndrome in an Unusual Age by Kursad Zengin, Mustafa Yasar Ozdamar, Sebahattin Albayrak, Serhat Tanik, Muhittin Atar, Hasan Bakirtas, Muhammed Abdurrahim Imamoglu, Mesut Gurdal

    Published 2015-01-01
    “…Therefore, we aimed to present a boy who is 8 years old diagnosed as PTS because of his mother’s hair coil.…”
    Get full text
    Article
  16. 776

    Plexiform Neurofibroma of the Submandibular Salivary Gland in a Child by Jacqueline M Bourgeois, Jasim Radhi, Lisa Elden, Gerald Gill

    Published 2001-01-01
    “…In the literature, most reported tumours have been present in the parotid gland region. A three-year-old boy with a family history of neurofibromatosis presented with a rapidly growing left submandibular mass. …”
    Get full text
    Article
  17. 777

    Management of a Severely Submerged Primary Molar: A Case Report by Iman Parisay, Fatemeh Kebriaei, Bentolhoda Varkesh, Milad Soruri, Roya Ghafourifard

    Published 2013-01-01
    “…In this case report, a five-year-old boy, who had a retained and submerged left lower second primary molar, was presented. …”
    Get full text
    Article
  18. 778

    Low-Grade Mucoepidermoid Carcinoma of the Lacrimal Gland in a Teenaged Patient by Ozgun Melike Gedar Totuk, Mustafa Kemal Demir, Ozlem Yapicier, Mert Mestanoglu

    Published 2017-01-01
    “…Herein, we report clinical and radiological findings of a mucoepidermoid carcinoma arising from the lacrimal gland in a 15-year-old boy. We suggest that since preoperative imaging findings are not diagnostic for mucoepidermoid carcinoma, histopathologic examination should be performed for definitive diagnosis. …”
    Get full text
    Article
  19. 779

    Dramatic Improvement of Subcutaneous Calcinosis by Intermittent, High-Dose Etidronate plus Cimetidine in a Patient with Juvenile Dermatomyositis by Takayuki Wakabayashi, Noriko Sasaki, Naofumi Chinen, Yasuo Suzuki

    Published 2015-01-01
    “…A 17-year-old boy with juvenile dermatomyositis presented with typical skin symptoms, mild myositis, and bilateral lower limb calcinosis. …”
    Get full text
    Article
  20. 780

    Validation of a hypomorphic variant in CDK13 as the cause of CHDFIDD with autosomal recessive inheritance through determination of an episignature by Jan Fischer, Mariëlle Alders, Marcel M. A. M. Mannens, David Genevieve, Karl Hackmann, Evelin Schröck, Bekim Sadikovic, Joseph Porrmann

    Published 2025-01-01
    “…Using the determination of a methylation pattern and comparison with an established episignature, we reveal the first hypomorphic variant in the kinase domain of CDK13, leading to a never before described autosomal recessive form of CHDFIDD in a boy with characteristic features. This highlights the utility of episignatures in variant interpretation, as well as a potential novel diagnostic approach in unsolved cases or for disease prognosis.…”
    Get full text
    Article