Pfeiffer Syndrome
- 1 March 1971
- journal article
- research article
- Published by American Medical Association (AMA) in American Journal of Diseases of Children
- Vol. 121 (3) , 257-262
- https://doi.org/10.1001/archpedi.1971.02100140123018
Abstract
A 4-year-old male child with acrocephaly, minimal syndactyly, broad thumbs and great toes, and normal intelligence is classified as having acrocephalosyndactyly type V, or Pfeiffer syndrome. This syndrome is compared with the other acrocephalosyndactyly types and the various broad thumb and great toe syndromes. These entities differ mainly in the type of digital anomaly, the craniofacial characteristics, the presence or absence of growth or mental retardation, and the mode of inheritance. The importance of diagnostic separation of these syndromes is stressed.Keywords
This publication has 4 references indexed in Scilit:
- The Rubinstein-Taybi SyndromeAmerican Journal of Diseases of Children, 1972
- The Rubinstein-Taybi syndrome: a report of two cases.Archives of Disease in Childhood, 1968
- Ein Beitrag zum Krankheitsbild der Akrocephalosyndaktylie (Apert)Archives of orthopaedic and trauma surgery, 1967
- Dominant erbliche AkrocephalosyndaktylieEuropean Journal of Pediatrics, 1964