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What is Miescher syndrome (2)?

What is Miescher syndrome (2)?

  • Miescher syndrome (2): A rare inherited disorder characterized by pigmented velvety patches of skin, excess body hair, failure to thrive, retarded growth, diabetes and facial abnormalities.

Miescher syndrome (2): Introduction

Types of Miescher syndrome (2):

Broader types of Miescher syndrome (2):

What causes Miescher syndrome (2)?

Causes of Miescher syndrome (2): see causes of Miescher syndrome (2)

What are the symptoms of Miescher syndrome (2)?

Symptoms of Miescher syndrome (2): see symptoms of Miescher syndrome (2)

Miescher syndrome (2): Testing

Diagnostic testing: see tests for Miescher syndrome (2).

Misdiagnosis: see misdiagnosis and Miescher syndrome (2).

How is it treated?

Doctors and Medical Specialists for Miescher syndrome (2): Medical Geneticist, Dermatologist ; see also doctors and medical specialists for Miescher syndrome (2).
Treatments for Miescher syndrome (2): see treatments for Miescher syndrome (2)

Name and Aliases of Miescher syndrome (2)

Main name of condition: Miescher syndrome (2)

Other names or spellings for Miescher syndrome (2):

Bloch-Miescher syndrome

 

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