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Oropharyngeal causes of swallowing difficulty and Developmental problems
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Contents
  1. Oropharyngeal causes of swallowing difficulty AND Developmental problems: Causes of All Symptoms
  2. Oropharyngeal causes of swallowing difficulty OR Developmental problems: 3842 causes
  3. Oropharyngeal causes of swallowing difficulty: Causes
  4. Oropharyngeal causes of swallowing difficulty: Introduction
  5. Developmental problems: 3841 causes
  6. Developmental problems: Introduction
  7. Oropharyngeal causes of swallowing difficulty and Developmental problems and Oropharyngeal causes of sucking and swallowing difficulty (3 causes)
  8. Oropharyngeal causes of swallowing difficulty and Developmental problems and Oropharyngeal causes of sucking difficulty (3 causes)
  9. Oropharyngeal causes of swallowing difficulty and Developmental problems and Sucking and swallowing difficulty (3 causes)
  10. Oropharyngeal causes of swallowing difficulty and Developmental problems and Sucking and swallowing difficulty in children (3 causes)
  11. Oropharyngeal causes of swallowing difficulty and Developmental problems and Sudden onset of swallowing difficulties in children (3 causes)
  12. Oropharyngeal causes of swallowing difficulty and Developmental problems and Body symptoms (2 causes)
  13. Oropharyngeal causes of swallowing difficulty and Developmental problems and Cleft palate (2 causes)
  14. Oropharyngeal causes of swallowing difficulty and Developmental problems and Deformity symptoms (2 causes)
  15. Oropharyngeal causes of swallowing difficulty and Developmental problems and Ear symptoms (2 causes)
  16. Oropharyngeal causes of swallowing difficulty and Developmental problems and Face deformity (2 causes)
  17. Oropharyngeal causes of swallowing difficulty and Developmental problems and MORE SYMPTOMS

Oropharyngeal causes of swallowing difficulty and Developmental problems

  • Oropharyngeal causes of swallowing difficulty AND Developmental problems - Causes of All Symptoms
  • Oropharyngeal causes of swallowing difficulty OR Developmental problems - 3842 causes

Oropharyngeal causes of swallowing difficulty:

Developmental problems:

Results: Causes of Oropharyngeal causes of swallowing difficulty AND Developmental problems

Results: 3842 causes of Oropharyngeal causes of swallowing difficulty OR Developmental problems

    1. +r(1) and +r(16)
     A very rare chromosomal disorder where some of the body's cells has extra ring chromosomes of chromosome 1 and chromosome 16....more »
    2. 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 »
    3. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    4. 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 »
    5. 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 »
    6. 2-Hydroxyglutaricaciduria
     A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...more »
    7. 2-Methylbutyric Aciduria
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    8. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    9. 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 »
    10. 2p21 deletion syndrome
     This syndrome is a more severe form hypotonia-cystinuria syndrome as a larger portion of genetic material from chromosome 2p21 is deleted. It is characterized by infant seizures, reduced muscle tone, developmental delay, lactic acidosis and unusual facial...more »

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  • Warning - Beta version - information may be incorrect (details)
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