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Symptom Checker » Dysarthria » Oropharyngeal and hypopharyngeal airway obstruction in newborns
 

Dysarthria and Oropharyngeal and hypopharyngeal airway obstruction in newborns
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Dysarthria and Oropharyngeal and hypopharyngeal airway obstruction in newborns

  • Dysarthria AND Oropharyngeal and hypopharyngeal airway obstruction in newborns - Causes of All Symptoms
  • Dysarthria OR Oropharyngeal and hypopharyngeal airway obstruction in newborns - 152 causes

Dysarthria:

Oropharyngeal and hypopharyngeal airway obstruction in newborns:

Results: Causes of Dysarthria AND Oropharyngeal and hypopharyngeal airway obstruction in newborns

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

Results: 152 causes of Dysarthria OR Oropharyngeal and hypopharyngeal airway obstruction in newborns

    1. Aceruloplasminemia
     A rare, recessively inherited neurodegenerative disorder characterized by a lack of ceruloplasmin in the blood. The lack of ceruloplasmin results in abnormal iron use in the body and leads to iron deposits in various body tissues such as the brain, pancre...more »
    2. Alcoholic cerebellar degeneration
     Cerebellar degeneration is a disease process in which the neurons in the cerebellum- the area of the brain that controls muscle co-ordination and balance- deteriorate and die....more »
    3. Alopecia -- hypogonadism -- extrapyramidal disorder
     A rare syndrome characterized by alopecia, progressive movement problems and a lack of gonadal function which affects puberty....more »
    4. Amyloidosis, oculoleptomeningeal
     Amyloidosis involves the abnormal deposit of a substance called amyloid in various parts of the body. In this particular type, the amyloid deposits in the leptomeningeal blood vessels, brainstem, spinal cord and eye causing central nervous system dysfunct...more »
    5. Amyotrophic lateral sclerosis
     A motor neuron disease involving progressive degeneration and eventual destruction of the function of nerves that control voluntary movement....more »
    6. Amyotrophic lateral sclerosis 3
     An inherited disorder involving progressive degeneration of motor neurons which results in muscle weakness and wasting. Type 3 is caused by a defect on chromosome 18q21....more »
    7. Amyotrophic lateral sclerosis 6
     An inherited disorder involving progressive degeneration of motor neurons which results in muscle weakness and wasting. Type 6 is caused by a defect on chromosome 16q12....more »
    8. Amyotrophic lateral sclerosis 7
     An inherited disorder involving progressive degeneration of motor neurons which results in muscle weakness and wasting. Type 7 is caused by a defect on chromosome 20p13....more »
    9. Amyotrophic lateral sclerosis 8
     An inherited disorder involving progressive degeneration of motor neurons which results in muscle weakness and wasting. Type 9 is caused by a defect on chromosome 20q13.3 and is a dominantly inherited, late-onset form....more »
    10. Anton-Vogt syndrome
     A congenital disorder where a brain anomaly results in involuntary purposeless movements (choreathetosis). Excitement and activity can make symptoms worse....more »

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