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Grant syndrome: A rare genetic condition characterized by short stature, skeletal abnormalities and blue sclerae. More detailed information about the symptoms, causes, and treatments of Grant syndrome is available below.
See full list of 11 symptoms of Grant syndrome
Home medical testing related to Grant syndrome:
Read more about causes of Grant syndrome.
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Read more about Misdiagnosis and Grant syndrome
Research related physicians and medical specialists:
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Research quality ratings and patient safety measures for medical facilities in specialties related to Grant syndrome:
Hospital & Clinic quality ratings »
Choosing the Best Hospital: More general information, not necessarily in relation to Grant syndrome, on hospital performance and surgical care quality:
Types of Grant syndrome
Read about other experiences, ask a question about Grant syndrome, or answer someone else's question, on our message boards:
Grant syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Grant syndrome, or a subtype of Grant 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 Grant syndrome as a "rare disease".
Source - Orphanet
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