VMJCR

A Genetic Echo in Enamel: Familial Hypoplastic Amelogenesis Imperfecta in a Young Female

Authors
  • Dr Shraddha Rasne Rasne

    Author
  • Dr. Lata M. Kale

    Author
  • Dr. Vishwas D. Kadam

    Author
  • Dr. Amruta Bansode

    Author
  • Dr. Preeti Baride

    Author
Keywords:
Amelogenesis imperfecta, Enamel hypoplasia, Hereditary dental disorder, Hypoplastic type, Prosthetic rehabilitation.
Abstract

Amelogenesis imperfecta (AI) is a group of inherited developmental disorders affecting enamel formation, resulting in structural and esthetic abnormalities of teeth. This case report describes a 19-year-old female with a positive family history suggesting a hereditary pattern.

The patient was treated by a multidisciplinary approach. This report highlights importance of early diagnosis and comprehensive treatment planning that are essential in managing AI to restore function, improve esthetics, and enhance the patient’s psychological well-being and quality of life.

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Published
2026-07-31
Section
Case Reports

How to Cite

A Genetic Echo in Enamel: Familial Hypoplastic Amelogenesis Imperfecta in a Young Female. (2026). Vittals Medicare Journal Of Case Reports. https://vmcasereports.com/vmjcr/article/view/30