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The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 1408
Calderon-Gonzalez-Cantu syndrome is characterized by the association of stubby, coarse, sparse and fragile hair, eyebrows and eyelashes with photosensitivity and nonprogressive intellectual deficit without a demonstrable metabolic aberration.
It has been described in three sisters born to consanguineous parents.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
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