Literature DB >> 31516772

Amelogenesis Imperfecta with Nephrocalcinosis: A Rare Association in Siblings.

Pramod Reddy1, Swathi Aravelli2, Soujanya Goud3, Loka Malathi4.   

Abstract

Enamel hypoplasia secondary to amelogenesis imperfect (AI) is one of the common developmental disturbances associated with the oral cavity. AI in association with multiple unerupted teeth is a rare entity, and in adolescence it not only has an affect on esthetics but also has an impact on the psychological status of the person. AI has been reported with other systemic anomalies previously. We report a case of AI in association with multiple unerupted teeth and nephrocalcinosis in siblings. The present case also highlights the importance of systemic examination and investigations in planning the treatment of a patient with AI.

Entities:  

Keywords:  amelogenesis imperfecta; enamel hypoplasia; nephrocalcinosis; retained deciduous teeth; unerupted teeth

Year:  2019        PMID: 31516772      PMCID: PMC6721873          DOI: 10.7759/cureus.5060

Source DB:  PubMed          Journal:  Cureus        ISSN: 2168-8184


  2 in total

1.  Enamel Renal Syndrome: Protocol for a Scoping Review.

Authors:  Imaan A Roomaney; Salma Kabbashi; Manogari Chetty
Journal:  JMIR Res Protoc       Date:  2021-11-30

2.  Enamel renal syndrome: A case report with review of literature.

Authors:  Ashish Sharma; Shubham Patel; Sasidhar Singaraju; Medhini Singaraju
Journal:  J Oral Maxillofac Pathol       Date:  2022-02-28
  2 in total

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