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The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
Orpha Number: 3387
A rare form of localised hypertrichosis characterised by hair growth near the laryngeal prominence during childhood.
This isolated anomaly has been described in around 20 individuals.
Transmission may be autosomal recessive or dominant with variable penetrance.
Visit the Orphanet disease page for more resources.
Source: GARD Last updated on 05-01-20
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