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Glossary for Ocular hypotelorism in children

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

  • Behavioral symptoms: Symptoms of personal behavior.
  • Child health symptoms: Symptoms related to pediatric (child) health.
  • Chromosome 20p, partial duplication: A rare chromosomal disorder where a copy of the short arm of chromosome 20 has been triplicated instead of duplicated resulting in various anomalies.
  • Cockayne syndrome: A rare genetic disorder characterized by a senile-like appearance, hearing and vision impairment and sun sensitive skin.
  • Coffin-Siris Syndrome: A rare genetic disorder characterized by underdeveloped or absent fifth finger and toenails and coarse facial features.
  • Cognitive impairment: General loss of mental or cognitive ability
  • Down Syndrome: A chromosome syndrome causing physical effects and mental retardation.
  • Eye symptoms: Symptoms affecting the eye
  • Face symptoms: Symptoms affecting the face
  • Goldenhar Syndrome: A congenital condition which affects the eyes, ears and vertebrae
  • Head symptoms: Symptoms affecting the head or brain
  • Maxillonasal dysplasia, Binder type: A rare disorder that may be inherited in some cases and is characterized by a distinctive face.
  • Meckel Syndrome: A rare genetic disorder involving numerous abnormalities and characterized by death within the first few weeks.
  • Microcephaly: A smaller than average brain
  • Ocular hypotelorism: Ocular hypotelorism is a condition in which there are abnormally wide-set eyes.
  • Ocular pain: Conditions of the eye which can cause pain.
  • Oculodentodigital syndrome: A rare genetic disorder characterized by small eyes, underdeveloped tooth enamel and permanent flexion of one or more finger joints.
  • Patau syndrome: A chromosomal disorder where there are three number 13 chromosomes as opposed to the normal two. The condition causes mental retardation and heart, kidney and scalp defects. Survival rate is very poor.
  • Say-Meyer syndrome: A very rare syndrome characterized mainly by short stature, developmental delay and trigonocephaly (premature fusion of skull bones giving the forehead a triangular shape).
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Skull symptoms: Symptoms affecting the skull surrounding the brain.
  • Turner Syndrome: Rare chromosome syndrome with one X but no second X or Y chromosome.
  • Williams Syndrome: A syndrome characterised by mental retardation, facial abnormalities and emotional instability
  • Wolf-Hirschorn syndrome: A syndrome characterised by the partial deletion of the short arm of chromosome 4

Conditions listing medical symptoms: Ocular hypotelorism in children:

The following list of conditions have 'Ocular hypotelorism 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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