The Unilateral Focal Dermal Hypoplasia - A Case Report and Literature Review
International Journal of Science and Research (IJSR)

International Journal of Science and Research (IJSR)
Call for Papers | Fully Refereed | Open Access | Double Blind Peer Reviewed

ISSN: 2319-7064


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Case Studies | Dentistry | India | Volume 14 Issue 2, February 2025 | Popularity: 5 / 10


     

The Unilateral Focal Dermal Hypoplasia - A Case Report and Literature Review

Dr. Nagendran J, Dr. Karthika Devaraj, Dr. Sarika Kannan


Abstract: Introduction: Focal dermal hypoplasia (FDH), formerly referred to as Goltz syndrome, is a rare multisystem condition characterised by an atypical genodermatosis which involves tissues derived from both ectoderm and mesoderm. It also affects various other tissues and organs, with the greatest impact on the connective tissue of the bones, skin, eyes, and oral cavity. Case presentation: A 7 - year - old female patient presented with a history of FDH exhibited a diverse range of systemic and oral manifestations. Extra and Intraoral examination showed Cutaneous changes along with facial asymmetry and few other oral manifestations including increase in incidence of caries and radiographic interpretation shows congenitally missing permanent teeth. Conclusion: This paper will enlighten the distinctive general and oral observations which will help the pediatric dentist to understand this rare clinical anomaly, formulating plans, and providing preventive and rehabilitative management.


Keywords: Focal dermal hypoplasia (FDH), Goltz syndrome. oral manifestation, polydactyly


Edition: Volume 14 Issue 2, February 2025


Pages: 1067 - 1070


DOI: https://www.doi.org/10.21275/SR25212000733


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Dr. Nagendran J, Dr. Karthika Devaraj, Dr. Sarika Kannan, "The Unilateral Focal Dermal Hypoplasia - A Case Report and Literature Review", International Journal of Science and Research (IJSR), Volume 14 Issue 2, February 2025, pp. 1067-1070, https://www.ijsr.net/getabstract.php?paperid=SR25212000733, DOI: https://www.doi.org/10.21275/SR25212000733

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