Beare-Stevenson cutis gyrata syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Beare-Stevenson cutis gyrata syndrome, or a subtype of Beare-Stevenson cutis gyrata syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Beare-Stevenson cutis gyrata syndrome: Introduction
Complications of Beare-Stevenson cutis gyrata syndrome:
see complications of Beare-Stevenson cutis gyrata syndrome
Symptoms of Beare-Stevenson cutis gyrata syndrome: see symptoms of Beare-Stevenson cutis gyrata syndrome
Complications of Beare-Stevenson cutis gyrata syndrome: see complications of Beare-Stevenson cutis gyrata syndrome
Onset of Beare-Stevenson cutis gyrata syndrome: birth
Treatments for Beare-Stevenson cutis gyrata syndrome:
see treatments for Beare-Stevenson cutis gyrata syndrome
Research for Beare-Stevenson cutis gyrata syndrome:
see research for Beare-Stevenson cutis gyrata syndrome
Main name of condition: Beare-Stevenson cutis gyrata syndrome
Other names or spellings for Beare-Stevenson cutis gyrata syndrome:Cutis Gyrata syndrome of Beare and Stevenson, cutis gyratra syndrome of Beare-Stevenson, Cutis gyratum acanthosis nigricans craniosynostosis, Beare-Stevenson syndrome
Cutis Gyrata syndrome of Beare and Stevenson, Beare stevenson syndrome
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
Research the causes of these diseases that are similar to, or related to, Beare-Stevenson cutis gyrata syndrome:
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