Hypomaturation amelogenesis imperfecta is a genetic tooth-enamel disorder. In this condition, the tooth builds a normal-thickness enamel layer during early development, but the final “maturation” ...
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 of each tooth. In type 2, the tooth ...
Enamel-renal-gingival syndrome is a rare inherited condition that affects the teeth, the kidneys, and the gums. Children are born with a gene change (they inherit it from both parents) that stops the ...
Enamel-renal syndrome is a very rare genetic condition. It affects the teeth and the kidneys at the same time. In the teeth, the hard outer layer (enamel) is very thin or almost absent. This is a ...
Amelogenesis imperfecta–gingival hyperplasia syndrome is a rare inherited condition that mainly affects the teeth and gums. “Amelogenesis imperfecta” means the enamel (the hard, shiny outer coating ...
Amelogenesis imperfecta hypoplastic with nephrocalcinosis is a rare, inherited condition. It mainly affects teeth and kidneys.In the teeth, the outer hard layer (enamel) is too thin or missing in ...
Amelogenesis imperfecta (AI) is a group of genetic conditions where the hard outer layer of the teeth, called enamel, does not form in the normal way. When AI is caused by a mutation in a gene named ...
Amelogenesis imperfecta and gingival fibromatosis syndrome is a rare, inherited condition that mainly affects the mouth and teeth. People are born with a problem in the way their tooth enamel forms ...
Oral and dental diseases include tooth decay (cavities), gum disease (periodontal disease), tooth loss, and oral cancer, which are largely preventable through good oral hygiene like brushing and ...
Enamel-Renal-Gingival Syndrome is a rare inherited condition that mainly affects the teeth, gums, and kidneys. Children are usually born healthy, but the enamel (the hard white outer layer of the ...
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, the enamel is very thin or even missing ...
X-linked amelogenesis imperfecta 1 is a genetic condition that affects how tooth enamel forms. “X-linked” means the change is on the X chromosome. The main gene involved is AMELX, which makes ...
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 a key enamel protein called ...
Snow-capped teeth describes a special look of tooth enamel where the biting edges of front teeth or the chewing tips of back teeth appear bright white and opaque, like snow on a mountain top. The ...
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 or harden normally before the tooth appears ...
Amelogenesis imperfecta (AI) is a group of genetic conditions that affect the hard outer cover of the teeth, called enamel. People with AI are born with enamel that is too thin, too soft, poorly ...
Amelogenesis imperfecta type 1E is a rare, inherited enamel disorder. It belongs to the hypoplastic group of amelogenesis imperfecta (AI), which means the enamel layer is too thin because not enough ...
Hypoplastic amelogenesis imperfecta is a genetic problem of tooth enamel formation. “Hypoplastic” means there is too little enamel. The enamel that forms is thin but usually properly mineralized ...
Amelogenesis imperfecta (AI) type 1 is the hypoplastic type of AI. That means the enamel is too thin or only partly formed from birth. Enamel is the hard, white outer layer that protects teeth. In ...
Bilingual aphasia is a language problem that happens after brain injury in a person who uses two languages.Aphasia means trouble using or understanding language because parts of the brain that handle ...
