What is Jaffer-Beighton syndrome?
What is Jaffer-Beighton syndrome?
- Jaffer-Beighton syndrome: A rare inherited syndrome characterized by loose joints, slipped vertebrae and long, thin fingers.
Jaffer-Beighton syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Jaffer-Beighton syndrome, or a subtype of Jaffer-Beighton 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 Jaffer-Beighton syndrome as a "rare disease".
Source - Orphanet
Jaffer-Beighton syndrome: Introduction
Types of Jaffer-Beighton syndrome:
Broader types of Jaffer-Beighton syndrome:
What causes Jaffer-Beighton syndrome?
Causes of Jaffer-Beighton syndrome: see causes of Jaffer-Beighton syndrome
What are the symptoms of Jaffer-Beighton syndrome?
Symptoms of Jaffer-Beighton syndrome:
see symptoms of Jaffer-Beighton syndrome
Jaffer-Beighton syndrome: Testing
Misdiagnosis: see misdiagnosis and Jaffer-Beighton syndrome.
How is it treated?
Doctors and Medical Specialists for Jaffer-Beighton syndrome: Medical Geneticist
;
see also doctors and medical specialists for Jaffer-Beighton syndrome.
Treatments for Jaffer-Beighton syndrome:
see treatments for Jaffer-Beighton syndrome
Name and Aliases of Jaffer-Beighton syndrome
Main name of condition: Jaffer-Beighton syndrome
Other names or spellings for Jaffer-Beighton syndrome:
arachnodactyly [loose joints - spondylolisthesis], Arachnodactyly, joint laxity, and spondylolisthesis
Arachnodactyly, joint laxity, and spondylolisthesis
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)