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Enamel hypoplasia
- Amelogenesis imperfecta is a tooth development disorder. It causes the tooth enamel to be thin and abnormally formed. Enamel is the ...
- ... of the disorder in their family. AI Congenital enamel hypoplasia Genetic Testing Registry: Amelogenesis imperfecta - hypoplastic autosomal dominant - ...
- Usher Syndrome (Genetic and Rare Diseases Information Center)Usher Syndrome/Learn More ... Usher Syndrome ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information ...
- Incontinentia Pigmenti (Genetic and Rare Diseases Information Center)Skin Pigmentation Disorders/Specifics ... Skin Pigmentation Disorders ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find ...
- Williams Syndrome (Genetic and Rare Diseases Information Center)Genetic Disorders/Specifics ... Genetic Disorders ... Developmental Disabilities/Specifics ... Developmental Disabilities ... Genetic and Rare Diseases Information Center ...
- ... symptoms may include thin enamel on the teeth (enamel hypoplasia) and chronic diarrhea or constipation associated with difficulty ...
- ... forms the protective outer layer of each tooth (enamel). Less commonly, abnormalities of the kidneys and gastrointestinal system are present. ...
- ... condition include mildly "coarse" facial features, thin tooth enamel, multiple cavities, heart valve abnormalities, a mildly enlarged liver (hepatomegaly), and a soft ...
- The ENAM gene provides instructions for making a protein called enamelin, which is essential for normal tooth development. Enamelin is involved in the formation ...
- ... delayed teething (dentition), misaligned teeth, and defective tooth enamel.Individuals with OFCD syndrome can have additional features, such as skeletal abnormalities (typically affecting the toes), hearing loss, and intellectual ...