Oral and dental diseases include tooth decay (cavities), gum disease (periodontal disease), tooth loss, and oral cancer, which are largely preventable through ...
Dr. Priya Kishnani, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
Enamel-Renal-Gingival Syndrome is a rare inherited condition that mainly affects the teeth, gums, and kidneys. Children are usually born healthy, but 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, ...
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 ...
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 ...
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 ...
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 ...
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 ...
Amelogenesis imperfecta type 1E is a rare, inherited enamel disorder. It belongs to the hypoplastic group of amelogenesis imperfecta (AI), which means the ...
Hypoplastic amelogenesis imperfecta is a genetic problem of tooth enamel formation. “Hypoplastic” means there is too little enamel. The enamel that forms is ...
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, ...
Amelogenesis imperfecta is a group of rare, inherited conditions where the outer white layer of the teeth (enamel) does not form normally. The problem starts ...
Kohlschütter–Tönz syndrome (KTS) is a very rare inherited condition. It usually starts in the first year of life. The key signs are: seizures (epilepsy), slow ...
Epilepsy–dementia–amelogenesis imperfecta syndrome is a genetic disease that a child gets when they inherit a faulty copy of a gene from both parents. The most ...
Amelocerebrohypohidrotic syndrome is a rare, inherited disorder. It mainly affects the teeth, the brain, and the sweat glands. Children usually begin to show ...
Ameloblastoma is a slow-growing tumor that starts from the cells that help form teeth (the enamel-making cells). It most often happens in the lower jaw ...
Ameloblastoma is a rare tumor that starts from the tooth-forming cells in the jaw. These cells are called ameloblasts, and they normally help make enamel. In ...
An odontoma is a benign (non-cancerous) growth made from the same hard tissues that build a normal tooth: enamel, dentin, cementum, and sometimes pulp. It ...
Ameloblastic carcinoma is a rare, aggressive cancer that starts from the tooth-forming epithelium inside the jaw bones (mandible or maxilla). It looks and ...
Forelimb non-syndromic amelia means a baby is born without one (or both) upper limb(s), and this happens by itself—not as part of a wider syndrome (like heart, ...
