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Symptom Checker » Anteverted nostrils » Prominent forehead
 

Anteverted nostrils and Prominent forehead and Skin texture changes and Speech symptoms and Throat symptoms and Tooth deformity
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Anteverted nostrils and Prominent forehead and Skin texture changes and Speech symptoms and Throat symptoms and Tooth deformity

  • Anteverted nostrils AND Prominent forehead AND Skin texture changes AND Speech symptoms AND Throat symptoms AND Tooth deformity - Causes of All Symptoms
  • Anteverted nostrils OR Prominent forehead OR Skin texture changes OR Speech symptoms OR Throat symptoms OR Tooth deformity - 4515 causes

Anteverted nostrils:

Prominent forehead:

Skin texture changes:

Speech symptoms:

Throat symptoms:

Tooth deformity:

Results: Causes of Anteverted nostrils AND Prominent forehead AND Skin texture changes AND Speech symptoms AND Throat symptoms AND Tooth deformity

Results: 4515 causes of Anteverted nostrils OR Prominent forehead OR Skin texture changes OR Speech symptoms OR Throat symptoms 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. 1q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    4. 1q terminal deletion
     A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    5. 22q11.2 deletion syndrome
     A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans....more »
    6. 2q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    7. 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 »
    8. 3-methylglutaconic aciduria, type 1
     A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine....more »
    9. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »
    10. 3q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 3 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »

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