VMJCR

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

लेखक

  • Dr Shraddha Rasne Rasne

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  • Dr. Lata M. Kale

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  • Dr. Vishwas D. Kadam

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  • Dr. Amruta Bansode

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  • Dr. Preeti Baride

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Amelogenesis imperfecta##common.commaListSeparator## Enamel hypoplasia##common.commaListSeparator## Hereditary dental disorder##common.commaListSeparator## Hypoplastic type##common.commaListSeparator## Prosthetic rehabilitation.
सार

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.

Cover Image
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प्रकाशित
2026-07-31
अंक
VOLUME 1| ISSUE 2| JULY-AUGUST 2026
खंड
Case Reports

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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