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Diseases » Fleisher syndrome » Summary
 

What is Fleisher syndrome?

What is Fleisher syndrome?

  • Fleisher syndrome: A rare inherited condition characterized by a deficiency of growth hormones and reduced blood levels of antibodies in the blood.

Fleisher syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Fleisher syndrome, or a subtype of Fleisher syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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

Fleisher syndrome: Introduction

Types of Fleisher syndrome:

Broader types of Fleisher syndrome:

What causes Fleisher syndrome?

Causes of Fleisher syndrome: see causes of Fleisher syndrome

What are the symptoms of Fleisher syndrome?

Symptoms of Fleisher syndrome: see symptoms of Fleisher syndrome

Fleisher syndrome: Testing

Diagnostic testing: see tests for Fleisher syndrome.

Misdiagnosis: see misdiagnosis and Fleisher syndrome.

How is it treated?

Doctors and Medical Specialists for Fleisher syndrome: Medical Geneticist ; see also doctors and medical specialists for Fleisher syndrome.
Treatments for Fleisher syndrome: see treatments for Fleisher syndrome

Name and Aliases of Fleisher syndrome

Main name of condition: Fleisher syndrome

Other names or spellings for Fleisher syndrome:

Nanism due to growth hormone isolated deficiency with X-linked hypogammaglobulinemia, isolated growth hormone deficiency type III, Agammaglobulinemia and Isolated growth hormone deficiency, X-linked, Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked, growth hormone deficiency [hypogammaglobulinemia], agammaglobulinemia [growth hormone deficiency], Isolated growth hormone deficiency, type 3

Isolated growth hormone deficiency, type III, Nanism due to growth hormone isolated deficiency with X linked hypogammaglobulinemia, Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked, Isolated growth hormone deficiency, type III, Nanism due to growth hormone isolated deficiency with X linked hypogammaglobulinemia, Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked, Agammaglobulinemia and isolated growth hormone deficiency, X-linked, Nanism due to growth hormone isolated deficiency with X linked hypogammaglobulinemia, Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked, Agammaglobulinemia and isolated growth hormone deficiency, X-linked, Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked, Agammaglobulinemia and isolated growth hormone deficiency, X-linked, Isolated growth hormone deficiency, type III
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Fleisher syndrome: Related Conditions

Research the causes of these diseases that are similar to, or related to, Fleisher syndrome:

 

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