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Amelogenesis imperfecta type 1G is a rare, inherited condition where the outer hard covering of the teeth (the enamel) does not form normally. In this type,...
Amelogenesis imperfecta type 2 is a genetic enamel formation problem that mainly affects the maturation stage of enamel. Your enamel is the hard, shiny outer layer...
Amelogenesis imperfecta (AI) is a group of rare, inherited conditions that affect the outer layer of the teeth, called enamel. In AI, enamel does not form...
Ameloonychohypohidrotic syndrome is an extremely rare condition that affects structures that come from the body’s outer layer (the ectoderm)—especially tooth enamel, nails, and sweat glands. People...
AMELX amelogenesis imperfecta is a hereditary (genetic) enamel problem caused by a change (mutation) in a gene called AMELX on the X-chromosome. The AMELX gene makes...
Anhidrotic Ectodermal Dysplasia with Immunodeficiency (EDA-ID) is a rare genetic disorder that affects various parts of the body, including the skin, hair, teeth, and immune system....
Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) is a rare genetic disorder that affects various parts of the body. In this simplified guide, we’ll provide you with clear explanations...
Ankyloglossia is a congenital condition characterized by an abnormally short, thickened, or tight lingual frenulum, or an anterior attachment of the lingual frenulum, that restricts the...
Anodontia is a rare dental condition where a person is born with missing teeth. This article will provide simple, easy-to-understand explanations for various aspects of anodontia,...
Anodontia means a person is born without any teeth at all. It is the most severe form of tooth agenesis, which is a developmental problem where...
Anosmia is a condition characterized by the partial or complete loss of the sense of smell. This impairment can significantly affect a person’s quality of life,...
Anotia means a baby is born without the outer ear (the visible ear on the side of the head). It is the most severe end of...
