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What is Morse-Rawnsley-Sargent syndrome?

What is Morse-Rawnsley-Sargent syndrome?

  • Morse-Rawnsley-Sargent syndrome: A very rare syndrome characterized mainly by abnormal brain development and reduced fetal movement.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Morse-Rawnsley-Sargent syndrome as a "rare disease".
Source - Orphanet

Morse-Rawnsley-Sargent syndrome: Introduction

Types of Morse-Rawnsley-Sargent syndrome:

Broader types of Morse-Rawnsley-Sargent syndrome:

How serious is Morse-Rawnsley-Sargent syndrome?

Complications of Morse-Rawnsley-Sargent syndrome: see complications of Morse-Rawnsley-Sargent syndrome

What causes Morse-Rawnsley-Sargent syndrome?

Causes of Morse-Rawnsley-Sargent syndrome: see causes of Morse-Rawnsley-Sargent syndrome

What are the symptoms of Morse-Rawnsley-Sargent syndrome?

Symptoms of Morse-Rawnsley-Sargent syndrome: see symptoms of Morse-Rawnsley-Sargent syndrome

Complications of Morse-Rawnsley-Sargent syndrome: see complications of Morse-Rawnsley-Sargent syndrome

Morse-Rawnsley-Sargent syndrome: Testing

Diagnostic testing: see tests for Morse-Rawnsley-Sargent syndrome.

Misdiagnosis: see misdiagnosis and Morse-Rawnsley-Sargent syndrome.

How is it treated?

Doctors and Medical Specialists for Morse-Rawnsley-Sargent syndrome: Obstetrician, Neonatologist ; see also doctors and medical specialists for Morse-Rawnsley-Sargent syndrome.
Treatments for Morse-Rawnsley-Sargent syndrome: see treatments for Morse-Rawnsley-Sargent syndrome

Name and Aliases of Morse-Rawnsley-Sargent syndrome

Main name of condition: Morse-Rawnsley-Sargent syndrome

Other names or spellings for Morse-Rawnsley-Sargent syndrome:

holoprosencephaly with fetal akinesia/hypokinesia sequence

 

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