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Diseases » Monosomy 1p36 » Summary

What is Monosomy 1p36?

What is Monosomy 1p36?

  • Monosomy 1p36: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as heart problems, mental retardation, developmental delay, facial dysmorphism and short stature. The range and severity of symptoms is variable with some cases being relatively mild.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Monosomy 1p36 as a "rare disease".
Source - Orphanet

Monosomy 1p36: Introduction

Types of Monosomy 1p36:

Broader types of Monosomy 1p36:

How serious is Monosomy 1p36?

Prognosis of Monosomy 1p36: The prognosis varies considerably depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.
Complications of Monosomy 1p36: see complications of Monosomy 1p36

What causes Monosomy 1p36?

Causes of Monosomy 1p36: see causes of Monosomy 1p36

What are the symptoms of Monosomy 1p36?

Symptoms of Monosomy 1p36: see symptoms of Monosomy 1p36

Complications of Monosomy 1p36: see complications of Monosomy 1p36

How is it treated?

Doctors and Medical Specialists for Monosomy 1p36: Medical Geneticist ; see also doctors and medical specialists for Monosomy 1p36.
Treatments for Monosomy 1p36: see treatments for Monosomy 1p36

Name and Aliases of Monosomy 1p36

Main name of condition: Monosomy 1p36

Other names or spellings for Monosomy 1p36:

Deletion 1p36


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