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Harrod syndrome
Disease definition
Harrod syndrome is characterized by the association of intellectual deficit, facial dysmorphism (a highly arched palate, pointed chin, and small mouth, hypotelorism, a long nose and large protruding ears), arachnodactyly, hypogenitalism (undescended testes and hypospadias) and failure to thrive.
ORPHA:2115
Classification level: DisorderSummary
Epidemiology
So far, it has been described in three males (including two brothers).
Etiology
The etiology remains unknown and an autosomal recessive mode of transmission has been suggested.
Additional information
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