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Dup(1) (q25-q32)

Dup(1) (q25-q32): Introduction

Dup(1) (q25-q32): A very rare chromosomal disorder where a portion of the long arm (q25-q32) of chromosome one is duplicated. The type and severity of symptoms may vary. More detailed information about the symptoms, causes, and treatments of Dup(1) (q25-q32) is available below.

Symptoms of Dup(1) (q25-q32)

Treatments for Dup(1) (q25-q32)

  • 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, facial abnormalities
  • 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 Dup(1) (q25-q32)?

Dup(1) (q25-q32): Complications

Review possible medical complications related to Dup(1) (q25-q32):

Causes of Dup(1) (q25-q32)

Read more about causes of Dup(1) (q25-q32).

Prognosis for Dup(1) (q25-q32)

Prognosis for Dup(1) (q25-q32): 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. Some patients die soon after birth due to severe malformations whereas others survive well into adulthood. The oldest reported survivor lived past 30 years of age.

Dup(1) (q25-q32): Broader Related Topics

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More information about Dup(1) (q25-q32)

  1. Dup(1) (q25-q32): Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
  6. Prognosis
 

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