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Diseases » WAGR Syndrome » Summary
 

What is WAGR Syndrome?

What is WAGR Syndrome?

  • WAGR Syndrome: A syndrome that is due to the deletion of chromosome 11.
  • WAGR Syndrome: A very rare congenital condition involving the complex of Wilms' tumor, aniridia, genitourinary abnormalities, and mental retardation. Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation (WAGR) syndrome involves hemizygous deletions of several adjacent genes in chromosome region 11p13. Two or more of the four conditions must be present for an individual to be diagnosed with WAGR Syndrome. The clinical picture varies, depending upon the combination of abnormalities. --2004
    Source - Diseases Database

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

WAGR Syndrome: Introduction

Types of WAGR Syndrome:

Broader types of WAGR Syndrome:

How serious is WAGR Syndrome?

Complications of WAGR Syndrome: see complications of WAGR Syndrome

What causes WAGR Syndrome?

Causes of WAGR Syndrome: see causes of WAGR Syndrome

What are the symptoms of WAGR Syndrome?

Symptoms of WAGR Syndrome: see symptoms of WAGR Syndrome

Complications of WAGR Syndrome: see complications of WAGR Syndrome

Onset of WAGR Syndrome: Many symptoms are present at birth. Wilms' tumor usually develops within the first few years of life.

WAGR Syndrome: Testing

Diagnostic testing: see tests for WAGR Syndrome.

Misdiagnosis: see misdiagnosis and WAGR Syndrome.

How is it treated?

Doctors and Medical Specialists for WAGR Syndrome: Medical Geneticist ; see also doctors and medical specialists for WAGR Syndrome.
Treatments for WAGR Syndrome: see treatments for WAGR Syndrome
Research for WAGR Syndrome: see research for WAGR Syndrome

Name and Aliases of WAGR Syndrome

Main name of condition: WAGR Syndrome

Other names or spellings for WAGR Syndrome:

11p- syndrome, 11p deletion syndrome, chromosome 11p monosomy, del (11p) syndrome, deletion 11p syndrome, monosomy 11p, partial monosomy 11p, aniridia type IV, aniridia-ambiguous genitalia-mental retardation (AGR) syndrome, triad, aniridia-genitourinary abnormalities-mental retardation triad, aniridia-Wilms tumor association, syndrome (aniridia-WT association, AWTA), aniridia-Wilms tumor-gonadoblastoma syndrome, dell 11/aniridia complex, oculocerebrorenal (OCR) syndrome, Brusa-Toricelli syndrome, Miller syndrome, Wilms tumor-aniridia syndrome, Wilms tumor-aniridia-genitourinary abnormalities-mental retardation triad, Wilms tumor-aniridia-gonadoblastoma-mental retardation (WAGR) syndrome, association, Wilms tumor, Aniridia, Genitourinary anomalies, mental Retardation syndrome, WAGR complex, Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome, Chromosome 11p deletion syndrome

11p deletion syndrome, Chromosome 11p deletion syndrome, WAGR Complex, Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome, Wilms tumor, Aniridia, Genitourinary anomalies, mental Retardation syndrome
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

WAGR Syndrome: Related Conditions

Research the causes of these diseases that are similar to, or related to, WAGR Syndrome:

 

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