Frontonasal dysplasia in two successive generations

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Abstract
Frontonasal dysplasia is thought to be a sporadic condition limited to the face and head. We describe a family from the Bahamas in which a mother, 2 of her children, and the mother's brother have variable manifestations of frontonassal dysplasia. The mother has extremely mild expression, but her brother and 2 sons are more severly affected. Besides polydactyly no other birth defects were noted in any other relatives. The pedigree is consistent with autosomal or X‐linked dominant inheritance. A description of each patient is presented along with a discussion of the genetic counseling issue and review of the literature for other possibly familial cases of frontonasal dysplasia.