Nephrocalcinosis in Amelogenesis Imperfecta Caused by the < b > < i > FAM20A < /i > < /b > Mutation

Conclusion: AI patients with similar clinical phenotypes andFAM20A mutations should be examined for nephropathy even if they lack pertinent symptoms. Nephrology referral is warranted for patients who have clinical phenotypes related to AI-gingival fibromatosis even if they are not symptomatic.Nephron
Source: Nephron - Category: Urology & Nephrology Source Type: research