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Symptoms » Preauricular tags » Glossary
 

Glossary for Preauricular tags

Medical terms related to Preauricular tags or mentioned in this section include:

  • 46,XX Gonadal dysgenesis epibulbar dermoid: A rare disorder characterized by gonad abnormalities and an eye disorder called epibulbar dermoid.
  • Bd syndrome: A very rare syndrome characterized mainly by the association of mental retardation, small eyes and a movement disorder.
  • Branchio oculo facial syndrome Hing type: A rare inherited disorder characterized by ear, eye and facial anomalies.
  • Cat Eye Syndrome: A rare chromosomal disorder involving abnormalities of chromosome 22 and characterized by coloboma of the iris, down-slanting palpebral fissures and anal atresia.
  • Chromosome 1, monosomy 1p32: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as mental retardation, clubfoot an umbilical hernia.
  • Chromosome 1, uniparental disomy 1q12 q21: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 11q duplication syndrome: A rare chromosomal disorder where there are three copies of the long arm (q) of chromosome 11 rather than the normal two resulting in various abnormalities. The type and severity of symptoms depend on the amount and location of genetic material duplicated.
  • Chromosome 13p duplication: A rare chromosomal disorder where duplication of a portion of chromosome 13 causes various abnormalities such as mental retardation, short stature, facial dysmorphism, delayed puberty and heart defects.
  • Chromosome 1p deletion syndrome: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 22 suprenumerary marker: A rare chromosomal disorder involving structural abnormalities of chromosome 22 and are more prevalent in children born to older mothers.
  • Chromosome 22, trisomy: A very rare disorder where there is an extra copy of chromosome 22 in all the body cells. The condition is usually fatal soon after birth or during the fetal stage.
  • Chromosome 4 Ring: A rare chromosomal disorder where the ends of chromosome 4 have been deleted and the two broken ends have rejoined to form a ring shape resulting in a range of symptoms determined by the size and location of the genetic deletion.
  • Chromosome 4 ring syndrome: A rare chromosomal disorder where the ends of chromosome 4 have been deleted and the two broken ends have rejoined to form a ring shape resulting in a range of symptoms determined by the size and location of the genetic deletion.
  • Chromosome 6, monosomy 6q: A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material.
  • Chromosome 6q deletion syndrome: A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material.
  • Del (3) (pter-25): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in 22 reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Del(1) (p36.1-p34.1): A very rare chromosomal disorder where a portion of the short arm (p36.1-p34.1) of chromosome one is missing. The type and severity of symptoms is variable.
  • Deletion 6q: A rare chromosomal disorder where a part of the long arm (q) of chromosome 6 is deleted resulting in various abnormalities depending on the location and length of missing genetic material.
  • Deletion of the Short Arm of Chromosome 1: A condition characterized by deletion of the short arm of chromosome 1
  • Developmental problems: Physical or mental development difficulty.
  • Dup (2) (pter-p23) and del (pter-p15): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in the few reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Ear symptoms: Symptoms affecting the ear or hearing
  • Face symptoms: Symptoms affecting the face
  • Head symptoms: Symptoms affecting the head or brain
  • Lambert syndrome: A rare syndrome characterized by a club foot, inguinal hernia, biliary atresia and branchial dysplasia.
  • Limb symptoms: Symptoms affecting the limbs
  • Macrostomia -- preauricular tags -- external ophthalmoplegia: A rare syndrome characterized mainly by a large mouth, skin tags in front of the ears and weak external eye muscles.
  • Megarbane-Loiselet syndrome: A rare syndrome characterized mainly by deafness and branchial anomalies.
  • Mental retardation athetosis microphthalmia: A very rare syndrome characterized mainly by the association of mental retardation, small eyes and a movement disorder.
  • Mouth symptoms: Symptoms of the mouth or oral area.
  • Oculo-oto-facial dysplasia: A rare syndrome characterized mainly by eye, ear and facial abnormalities.
  • Skin problems: Any condition that affects the skin
  • Skin symptoms: Symptoms affecting the skin.

Conditions listing medical symptoms: Preauricular tags:

The following list of conditions have 'Preauricular tags' 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.

Select from the following alphabetical view of conditions which include a symptom of Preauricular tags or choose View All.

 

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