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Symptom Checker » Abnormal eye movements » Anteverted nostrils
 

Abnormal eye movements and Anteverted nostrils and Hyperextensible joints and Prominent forehead and Skin texture changes and Tooth deformity
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Abnormal eye movements and Anteverted nostrils and Hyperextensible joints and Prominent forehead and Skin texture changes and Tooth deformity

  • Abnormal eye movements AND Anteverted nostrils AND Hyperextensible joints AND Prominent forehead AND Skin texture changes AND Tooth deformity - Causes of All Symptoms
  • Abnormal eye movements OR Anteverted nostrils OR Hyperextensible joints OR Prominent forehead OR Skin texture changes OR Tooth deformity - 1405 causes

Abnormal eye movements:

Anteverted nostrils:

Hyperextensible joints:

Prominent forehead:

Skin texture changes:

Tooth deformity:

Results: Causes of Abnormal eye movements AND Anteverted nostrils AND Hyperextensible joints AND Prominent forehead AND Skin texture changes AND Tooth deformity

Results: 1405 causes of Abnormal eye movements OR Anteverted nostrils OR Hyperextensible joints OR Prominent forehead OR Skin texture changes OR Tooth deformity

    1. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    2. 18p minus syndrome
     A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material t...more »
    3. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    4. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »
    5. 47,XXX syndrome
     A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomati...more »
    6. 8p-Syndrome, partial
     A rare chromosomal disorder where there is one copy of part of the short arm (p) of chromosome 8 rather than the normal two. The type and severity of symptoms is determined by the location and size of the genetic material deleted....more »
    7. Aarskog Syndrome
     A rare genetic condition characterized by facial, hand, genital and growth abnormalities....more »
    8. Abetalipoproteinemia
     A rare disorder involving abnormalities in fat metabolism. The resulting insufficiency of fats and vitamins affect the normal development and function of the body....more »
    9. Ablepharon macrostomia syndrome
     A rare disorder involving a number of mainly physical abnormalities....more »
    10. Ablinism I syndrome
     A recessively inherited form of albinism involving the complete lack of skin, hair and eye pigments....more »

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