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Glossary for Incisor abnormalities in children

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

  • 47 XYY syndrome: A genetic condition where males have an extra Y chromosome in each of their cells. Normally male cells have one X and one Y chromosome. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomatic.
  • Body symptoms: Symptoms affecting the entire body features.
  • Breath symptoms: Breath-related symptoms including breath odor
  • Breathing symptoms: Symptoms affecting the breathing systems.
  • Cataract dental syndrome: A very rare inherited condition mainly involving eye abnormalities but also various other physical abnormalities. The type and severity of symptoms is variable.
  • Child health symptoms: Symptoms related to pediatric (child) health.
  • Cleft lip: A condition which is characterized by a congenital cleft of the upper lip
  • Cleft palate: This when there is a congenital fissure of the median line of the palate.
  • 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.
  • Face symptoms: Symptoms affecting the face
  • Head symptoms: Symptoms affecting the head or brain
  • Hypopituitarism: A condition characterized by diminished hormonal section by the pituitary gland
  • Incontinentia Pigmenti: A rare genetic skin pigmentation disorder characterized by eye, teeth, bone, nail and hair malformations as well as central nervous abnormalities and mental deficiency.
  • Infant symptoms: Symptoms affecting babies and infants.
  • 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.
  • Poland Syndrome: A rare genetic disorder characterized by hand syndactyly and abnormality of one chest muscle.
  • Pregnancy symptoms: Symptoms related to pregnancy.
  • Respiratory symptoms: Symptoms affecting the breathing systems.
  • Rubinstein-Taybi Syndrome: A rare congenital disorder characterized by very small stature, broad thumbs and toes, slanted palpebral fissures and hypoplastic maxilla.
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Sturge-Weber Syndrome: A rare genetic disorder characterized by excessive blood vessel growth, calcium accumulation inside the brain and seizures.
  • Throat symptoms: Symptoms affecting the throat

Conditions listing medical symptoms: Incisor abnormalities in children:

The following list of conditions have 'Incisor abnormalities 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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