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Diseases » Monosomy 13q32 » Summary
 

What is Monosomy 13q32?

What is Monosomy 13q32?

  • Monosomy 13q32: A rare chromosomal disorder where a portion of the long arm (q32) of chromosome 13 is deleted resulting in various physical, neurological and developmental abnormalities. The type and severity of symptoms can vary amongst patients.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Monosomy 13q32 as a "rare disease".
Source - Orphanet

Monosomy 13q32: Introduction

Types of Monosomy 13q32:

Broader types of Monosomy 13q32:

How serious is Monosomy 13q32?

Prognosis of Monosomy 13q32: 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.

What causes Monosomy 13q32?

Causes of Monosomy 13q32: see causes of Monosomy 13q32

What are the symptoms of Monosomy 13q32?

Symptoms of Monosomy 13q32: see symptoms of Monosomy 13q32

How is it treated?

Doctors and Medical Specialists for Monosomy 13q32: Medical Geneticist ; see also doctors and medical specialists for Monosomy 13q32.
Treatments for Monosomy 13q32: see treatments for Monosomy 13q32

Name of Monosomy 13q32

Main name of condition: Monosomy 13q32

 

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