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Articulation disorders causing receptive and expressive language disorders in children and Deformity symptoms and Dental symptoms
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Articulation disorders causing receptive and expressive language disorders in children and Deformity symptoms and Dental symptoms

  • Articulation disorders causing receptive and expressive language disorders in children AND Deformity symptoms AND Dental symptoms - Causes of All Symptoms
  • Articulation disorders causing receptive and expressive language disorders in children OR Deformity symptoms OR Dental symptoms - 2307 causes

Articulation disorders causing receptive and expressive language disorders in children:

Deformity symptoms:

Dental symptoms:

Results: Causes of Articulation disorders causing receptive and expressive language disorders in children AND Deformity symptoms AND Dental symptoms

Note: Do not use for diagnosis; see limitations of results.

Results: 2307 causes of Articulation disorders causing receptive and expressive language disorders in children OR Deformity symptoms OR Dental symptoms

    1. 10q Partial Trisomy
     A very rare genetic disorder characterized by the duplication of genetic material from the long arm (q) of chromosome 10 - the genetic material occurs three times in body cells instead of the normal two. The type and severity of symptoms may vary consider...more »
    2. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    3. 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 »
    4. 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 »
    5. 1q proximal deletion
     A rare chromosomal disorder where the proximal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    6. 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 »
    7. 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 »
    8. 2q22-q24 deletion
     A rare chromosomal disorder where part of the long arm (q22-q24) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    9. 3-M Syndrome
     A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected....more »
    10. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....more »

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  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
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