110 top medical experts on Amelogenesis imperfecta nephrocalcinosis across 11 countries and 1 U.S. states, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Amelogenesis imperfecta nephrocalcinosis: A extremely rare, genetic malformation syndrome characterized by hypoplastic amelogenesis imperfecta (hypoplastic dental enamel) and nephrocalcinosis (precipitation of calcium salts in renal tissue). Oral manifestations include yellow and misshaped teeth, delayed tooth eruption, and intrapulpal calcifications. Nephrocalcinosis is often asymptomatic but can progress during late childhood or early adulthood to impaired renal function, recurrent urinary infections, renal tubular acidosis, and rarely to end-stage renal failure.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: nephrocalcinosis and apparently normal calcium metabolism Absent enamel,  and Nephrocalcinosis Hypoplastic Amelogenesis Imperfecta,  Type IG Amelogenesis Imperfecta,  Enamel renal syndrome,  Enamel-Renal Syndrome,  Generalized enamel hypoplasia and renal dysfunction


  

        

                    


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