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Del(1) (p22.3-p13.3)

Del(1) (p22.3-p13.3): Introduction

Del(1) (p22.3-p13.3): A very rare chromosomal disorder where a portion of the short arm (p22.3-p13.3) of chromosome one is missing. The type and severity of symptoms is variable. More detailed information about the symptoms, causes, and treatments of Del(1) (p22.3-p13.3) is available below.

Symptoms of Del(1) (p22.3-p13.3)

Treatments for Del(1) (p22.3-p13.3)

  • Treatment varies depending on the type and severity of symptom that develop:
  • Surgery may be needed to correct defects or abnormalities e.g. heart defects
  • Access to programs and services as required e.g. physical therapy, speech therapy, educational support, social, vocational and medical services
  • Various symptomatic and supportive measures as required
  • Genetic counseling and joining a support group is recommended
  • more treatments...»

Wrongly Diagnosed with Del(1) (p22.3-p13.3)?

Del(1) (p22.3-p13.3): Complications

Review possible medical complications related to Del(1) (p22.3-p13.3):

Causes of Del(1) (p22.3-p13.3)

Read more about causes of Del(1) (p22.3-p13.3).

Prognosis for Del(1) (p22.3-p13.3)

Prognosis for Del(1) (p22.3-p13.3): The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.

Del(1) (p22.3-p13.3): Broader Related Topics

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More information about Del(1) (p22.3-p13.3)

  1. Del(1) (p22.3-p13.3): Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
  6. Prognosis

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