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Dyschromatosis Universalis Hereditaria 1

Dyschromatosis Universalis Hereditaria 1: Introduction

Dyschromatosis Universalis Hereditaria 1: Dyschromatosis universalis is an inherited skin condition characterized by the progressive development of mottled skin made up of small areas of increased and decreased skin pigmentation. The trunk is the main area of skin affected but the limbs and sometimes the face may also be involved. Subtype 1 is the result of a defect on chromosome 6q24.2-q25.2. More detailed information about the symptoms, causes, and treatments of Dyschromatosis Universalis Hereditaria 1 is available below.

Symptoms of Dyschromatosis Universalis Hereditaria 1

  • Mottled changes in skin pigmentation - can affect any part of the body
  • more symptoms...»

Wrongly Diagnosed with Dyschromatosis Universalis Hereditaria 1?

Causes of Dyschromatosis Universalis Hereditaria 1

Read more about causes of Dyschromatosis Universalis Hereditaria 1.

Misdiagnosis and Dyschromatosis Universalis Hereditaria 1

Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer from the skin disorder called psoriasis can often go undiagnosed. The main problem is that...read more »

Dyschromatosis Universalis Hereditaria 1: Research Doctors & Specialists

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Dyschromatosis Universalis Hereditaria 1: Animations

Prognosis for Dyschromatosis Universalis Hereditaria 1

Prognosis for Dyschromatosis Universalis Hereditaria 1: The skin mottling stops progressing before the adolescent years.

Dyschromatosis Universalis Hereditaria 1: Broader Related Topics

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Related Dyschromatosis Universalis Hereditaria 1 Info

More information about Dyschromatosis Universalis Hereditaria 1

  1. Dyschromatosis Universalis Hereditaria 1: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Prognosis
 

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