Rare Diseases Symptoms Automatic Extraction

Dentin dysplasia type I--a case report.

[dentin dysplasia]

A case report on dentin dysplasia type I, a congenital disease (autosomal dominant gene defect) affecting deciduous and permanent teeth, is depicted including representations of clinical and histological features, X-ray and CT-findings. Therapy includes extraction of all teeth, ectomization of cystic alteration, revision of paranasal sinus. Aesthetic and functional rehabilitation by means of insertion of a complete denture was achieved.

Diseases presenting "congenital disease" symptom

  • achondroplasia
  • coats disease
  • congenital toxoplasmosis
  • dentin dysplasia
  • hirschsprung disease
  • holt-oram syndrome
  • homocystinuria without methylmalonic aciduria
  • lamellar ichthyosis
  • megacystis-microcolon-intestinal hypoperistalsis syndrome
  • oligodontia
  • omenn syndrome

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