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PedAM

Pediatric Disease Annotations & Medicines




Disease neuropathy
Phenotype C0015464|facial palsy
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PubMedID- 20597346 It's typical initial manifestation is lattice corneal dystrophy, detected at biomicroscopic examination of the eye by the age of 25 to 30 years, followed by slowly progressing cranial neuropathy with bilateral facial palsy, polyneuropathy and generalized cutis laxa.

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