Glossary for Taurodontia in children

Medical terms related to Taurodontia in children or mentioned in this section include:

• 49,XXXXY syndrome: A rare sex chromosome abnormality where there are three extra copies of the X chromosome.
• Ackerman syndrome: An extremely rare condition characterized primarily by glaucoma, upper lip deformity and abnormal tooth roots.
• Apert syndrome: A rare condition characterized by abnormalities in the appearance of the face and head as well as finger and toe abnormalities. The bones of the skull fuse together too early which prevents it from growing normally. Various toes and fingers may be fused together.
• Behavioral symptoms: Symptoms of personal behavior.
• Breath symptoms: Breath-related symptoms including breath odor
• Breathing symptoms: Symptoms affecting the breathing systems.
• Child health symptoms: Symptoms related to pediatric (child) health.
• Cognitive impairment: General loss of mental or cognitive ability
• Dental symptoms: Symptoms affecting teeth or mouth area.
• Developmental problems: Physical or mental development difficulty.
• Down Syndrome: A chromosome syndrome causing physical effects and mental retardation.
• Dyskeratosis congenita of Zinsser-Cole-Engman: An inherited condition characterized by recurring painful mouth ulcers, skin pigmentation and nail abnormalities.
• Ectodermal dysplasia: A group of rare inherited conditions which affect the ectodermal skin layer which includes the skin, hair, teeth and nails.
• Face symptoms: Symptoms affecting the face
• Fragile-X Syndrome: A rare inherited characterized by various physical anomalies as well as mental retardation. The symptoms are milder in females.
• Head symptoms: Symptoms affecting the head or brain
• Klinefelter syndrome: A genetic condition where males have at least one extra X chromosome or extra copies of both the X and Y chromosomes in each cell. Normally male cells contain one X and one Y chromosome in each cell. The condition is not inherited but is a result of problems during cell division. Klinefelter syndrome variants is a more severe form of the condition as it involves more than one extra X or X and Y chromosome in each cell.
• Mouth symptoms: Symptoms of the mouth or oral area.
• Nevoid basal cell carcinoma syndrome: A rare genetic disorder characterized by basal cell carcinomas, broade face and rib abnormalities.
• Orofaciodigital syndrome type I:
• Otodental dysplasia: A very rare syndrome characterized mainly by ear and tooth abnormalities. The back teeth are large and have bulbous crowns without the normal grooves and features.
• Respiratory symptoms: Symptoms affecting the breathing systems.
• Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
• Throat symptoms: Symptoms affecting the throat
• Tricho-dento-osseous syndrome: A rare genetic disorder characterized by kinky hair, tooth enamel and bone abnormalities. There are two different subtypes with type I being distinguished from type II by the presence of a small head and increased density in the long bones.

Conditions listing medical symptoms: Taurodontia in children:

The following list of conditions have 'Taurodontia in children' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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