Abstract
Ectodermal Dysplasia (ED) is a rare genetic disorder characterized by the aberrant development of ectodermal structures, presenting complex dental, dermatological, and psychological challenges. This case report focuses on a 7-year-old male with ED, delving into his prenatal, natal, and postnatal history, medical and dental records, clinical examination findings, and the subsequent treatment plan. The patient exhibited classical ED features, including missing teeth, dry and fragile skin, prominent lips, cranial abnormalities, reduced facial height, and an enlarged tongue. A multidisciplinary team approach was pivotal in addressing the intricate dental complications associated with ED. Preventive measures such as meticulous oral hygiene, periodic high-fluoride applications, and resin-modified glass ionomer fissure sealants were administered. Prosthodontic interventions were designed to restore function and aesthetics, including upper partial denture and lower overdenture. This case underscores the significance of early and comprehensive dental intervention in ED patients, emphasizing the vital roles played by pediatrics, orthodontics, prosthodontics, surgery, and periodontics in achieving favorable outcomes. Furthermore, it highlights the psychosocial challenges faced by ED individuals, emphasizing the need for holistic care and support.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
