A case of Fryns syndrome
- PMID: 3950939
- PMCID: PMC1049547
- DOI: 10.1136/jmg.23.1.82
A case of Fryns syndrome
Abstract
A case of Fryns syndrome is presented. Characteristic features of this lethal autosomal recessive disorder include corneal clouding, camptodactyly with hypoplastic nails, and abnormalities of the diaphragm.
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