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Specialty: Endocrinology: Symptoms: Enlargement of the hands, feet, forehead, jaw, and nose, thicker skin, deepening of the voice [3]: Complications: Type 2 diabetes, sleep apnea, high blood pressure, [3] high cholesterol, heart problems, particularly enlargement of the heart (cardiomegaly), osteoarthritis, spinal cord compression or fractures, increased risk of cancerous tumors, precancerous ...
The formation of teeth begins during embryonic development and is a process that is highly regulated by various signaling pathways, which, if disrupted as a result of genetic mutations or environmental factors, can lead to developmental anomalies, including hyperdontia. Tooth development begins with the formation of tooth buds in the jaw.
Hypercementosis is an idiopathic, non-neoplastic condition characterized by the excessive buildup of normal cementum (calcified tissue) on the roots of one or more teeth. [1] A thicker layer of cementum can give the tooth an enlarged appearance, mainly occurring at the apex or apices of the tooth.
More colloquially, the condition may be referred to as gap teeth or tooth gap. In humans, the term is most commonly applied to an open space between the upper incisors (front teeth). It happens when there is an unequal relationship between the size of the teeth and the jaw. Diastemata are common for children and can exist in adult teeth as well.
Oromandibular dystonia is characterized by involuntary spasms of the tongue, jaw, and mouth muscles that result in bruxism, or grinding of the teeth, and jaw closure. These conditions frequently lead to secondary dental wear as well as temporomandibular joint syndrome. In addition, problems with chewing, speaking, and swallowing may result from ...
In the generalized form, all teeth are involved. In the localized form, only a few teeth are involved. The most common teeth affected are the upper lateral incisors and third molars. Teeth affected by microdontia may also have abnormal shape, and the abnormal size may affect the whole tooth, or only a part of the tooth. [1]
This is a common method of treatment for those with medium to mid-severe cases of macrodontia. [citation needed] A last-method approach to combat macrodontia is also to simply remove the affected tooth to make more space for the neighboring teeth. By doing so, this will make the teeth appear less crowded and smaller.
Axenfeld–Rieger syndrome is a rare autosomal dominant [2] disorder, which affects the development of the teeth, eyes, and abdominal region. [3]Axenfeld–Rieger syndrome is part of the so-called iridocorneal or anterior segment dysgenesis syndromes, [4] which were formerly known as anterior segment cleavage syndromes, anterior chamber segmentation syndromes or mesodermal dysgenesis.