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What is Frints -- De Smet -- Fabry -- Fryns syndrome?

What is Frints -- De Smet -- Fabry -- Fryns syndrome?

  • Frints -- De Smet -- Fabry -- Fryns syndrome: A rare syndrome characterized by a variation of Larsen syndrome where the physical manifestations are asymmetrical. This is believed to be a mosaic form of the genetic condition where the genetic anomaly is present in only some of the body's cells leading to asymmetric manifestations.

Frints -- De Smet -- Fabry -- Fryns syndrome: Introduction

Types of Frints -- De Smet -- Fabry -- Fryns syndrome:

Broader types of Frints -- De Smet -- Fabry -- Fryns syndrome:

What causes Frints -- De Smet -- Fabry -- Fryns syndrome?

Causes of Frints -- De Smet -- Fabry -- Fryns syndrome: see causes of Frints -- De Smet -- Fabry -- Fryns syndrome

What are the symptoms of Frints -- De Smet -- Fabry -- Fryns syndrome?

Symptoms of Frints -- De Smet -- Fabry -- Fryns syndrome: see symptoms of Frints -- De Smet -- Fabry -- Fryns syndrome

Frints -- De Smet -- Fabry -- Fryns syndrome: Testing

Misdiagnosis: see misdiagnosis and Frints -- De Smet -- Fabry -- Fryns syndrome.

How is it treated?

Doctors and Medical Specialists for Frints -- De Smet -- Fabry -- Fryns syndrome: Medical Geneticist ; see also doctors and medical specialists for Frints -- De Smet -- Fabry -- Fryns syndrome.
Treatments for Frints -- De Smet -- Fabry -- Fryns syndrome: see treatments for Frints -- De Smet -- Fabry -- Fryns syndrome

Name and Aliases of Frints -- De Smet -- Fabry -- Fryns syndrome

Main name of condition: Frints -- De Smet -- Fabry -- Fryns syndrome

Other names or spellings for Frints -- De Smet -- Fabry -- Fryns syndrome:

symbrachydactyly of the hand and foot, De Smet-Fabry-Fryns syndrome, Larsen Syndrome with asymmetric manifestation, Symbrachydactyly of hands and feet

 

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