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Symptoms » Enophthalmos » Glossary
 

Glossary for Enophthalmos

Medical terms related to Enophthalmos or mentioned in this section include:

  • Abnormal blood test symptoms: Abnormal results from diagnostic blood tests.
  • Accidental Eye Injury: The accidental injury to an eye
  • Blood symptoms: Symptoms affecting the blood and its blood cells.
  • Blurred vision: Blurriness of vision or images.
  • Body symptoms: Symptoms affecting the entire body features.
  • Chromosome 10, Monosomy 10p:
  • Chromosome 10p deletion syndrome: A rare chromosomal disorder where there is a deletion of the short arm (p) of chromosome 10 resulting in variable abnormalities.
  • Chromosome 9, Tetrasomy 9p: A rare chromosomal disorder where there is four copies of the short arm of chromosome 9 instead of the normal two resulting in various abnormalities.
  • Chromosome 9, trisomy 9p: A rare chromosomal disorder where a portion of the short arm (p) of chromosome 9 is duplicated so there is three copies of it instead of the normal two.
  • Chromosome 9p tetrasomy syndrome: A rare chromosomal disorder where there is four copies of the short arm of chromosome 9 instead of the normal two resulting in various abnormalities.
  • Dehydration: Loss and reduction in body water levels
  • Electrolyte imbalance symptoms: Symptoms related to an imbalance of the electrolyte levels in the blood.
  • Enophthalmos in children: Enophthalmos in children refers to the recession of a child's eyeball into the orbit of the skull.
  • Exudative retinopathy familial, X-linked, recessive: A rare progressive eye disorder which is inherited in a recessive X-linked manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function. The disorder is caused by a genetic defect on chromosome 11q14-q21 and the severity of the condition.
  • Exudative retinopathy familial, autosomal dominant: A rare progressive eye disorder which is inherited in a dominant manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function. The disorder is caused by a genetic defect on chromosome 11q14-q21 and the severity of the condition is variable.
  • Exudative retinopathy familial, autosomal recessive: A rare progressive eye disorder which is inherited in a recessive manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function.
  • Exudative retinopathy, familial: A rare progressive eye disorder which is inherited in a familial manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function.
  • Exudative vitreoretinopathy 3: A rare progressive eye disorder caused by a genetic defect on chromosome 11p13-p12. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function.
  • Exudative vitreoretinopathy 4: A rare progressive eye disorder caused by a genetic defect on chromosome 11q13.4. It can be inherited in a dominant or recessive manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function.
  • Eye symptoms: Symptoms affecting the eye
  • Face symptoms: Symptoms affecting the face
  • Head symptoms: Symptoms affecting the head or brain
  • Horner's syndrome: Horner's syndrome is characterised by ptosis, meiosis, anhidrosis and loss of ciliospinal reflex.
  • Injury: Any damage inflicted in the body
  • Marfan's syndrome: A genetic connective tissue disorder involving a defect of chromosome 15q21.1 which affects the production of the fibrillin needed to make connective tissue.
  • Nanophthalmos 2: A dominantly inherited eye disorder linked to a defect on chromosome 11q23 which results in very small eyes. The condition is usually associated with an increased risk of glaucoma.
  • Nanophthalmos 3: A dominantly inherited eye disorder linked to a defect on chromosome 2q11-q14 which results in very small eyes. The condition is usually associated with an increased risk of glaucoma.
  • Parry Romberg Syndrome: Wasting away of one side of the face.
  • RHYNS syndrome: A rare syndrome characterized by eye, kidney and skeletal abnormalities as well as hypopituitarism.
  • Silent sinus syndrome: The silent sinus syndrome refers to the collapse of the orbital floor and maxillary sinus which can cause changes in facial appearance. The condition is quite uncommon and usually causes no pain when it occurs. It is believed that the condition is often undiagnosed or misdiagnosed. The cause of the condition is not fully understood but is believed to be an acquired condition in most cases.
  • Sunken eye: Sunken eye is a eye that appears to be more recessed in the skull than normal.
  • Sunken eyes: The occurrence of eyes of an individual that appear to be sunken in nature
  • Vision changes: Any change in vision or sight.
  • Wasting Syndrome: AIDS related wasting syndrome is the involuntary loss of more than 10% of the body weight plus more than 30 days of either diarrhoea or weakness and fever. It is linked to disease progression and death.

Conditions listing medical symptoms: Enophthalmos:

The following list of conditions have 'Enophthalmos' 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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Conditions listing medical complications: Enophthalmos:

The following list of medical conditions have 'Enophthalmos' or similar listed as a medical complication in our database.

 

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