Apert syndrome with partial preaxial polydactyly.

Article

Apert syndrome with partial preaxial polydactyly.

Genetic counseling (Geneva, Switzerland) - 1 Jan 1992

Lefort G, Sarda P, Humeau C, Rieu D

Abstract excerpt

Acrocephalosyndactyly type I or Apert syndrome is characterized by craniosynostosis, particular dysmorphic features and abnormalities of the hands and feet. Rarely, polydactyly of the toes has been reported, and in this event the diagnosis of Carpenter syndrome must be discussed. A case of atypic...

Topics

Acrocephalosyndactylia
Craniosynostoses
Female
Genetic Counseling
Humans
Infant
Intellectual Disability
Phenotype

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