The acrocephalosyndactyly syndromes: A metacarpophalangeal pattern profile analysis
- 23 April 2008
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 11 (3) , 295-305
- https://doi.org/10.1111/j.1399-0004.1977.tb01316.x
Abstract
Metacarpophalangeal pattern profile (MCPP) analysis was applied to patients with Pfeiffer and Chotzen syndromes, dominantly inherited types of acrocephalosyndactyly (ACS). A characteristic MCPP was obtained for the group. However, it did not discriminate between patients with Chotzen syndrome and those with Pfeiffer syndrome. Six patients in a single family showing Pfeiffer syndrome exhibited this unique MCPP profile which was not present in non-affected family members. Furthermore, 3 normal-appearing relatives were identified as affected by this technique, and this diagnosis was subsequently confirmed by radiographic and genetic data. The MCPP in Pfeiffer and Chotzen syndromes is unique and can be used to make the diagnosis of an ACS syndrome in persons who show few or no clinical stigmata of disease. The MCPP does not discriminate between these 2 ACS types.This publication has 14 references indexed in Scilit:
- Unusual association of Saethre‐Chotzen syndrome and congenital adrenal hyperplasiaClinical Genetics, 1977
- A sporadic case of apparent Crouzon's syndrome with extracraniofacial manifestationsJournal of Medical Genetics, 1974
- Metacarpophalangeal Length in the Evaluation of Skeletal MalformationRadiology, 1972
- Metacarpophalangeal Pattern Profiles in the Evaluation of Skeletal MalformationsRadiology, 1972
- Pfeiffer SyndromeAmerican Journal of Diseases of Children, 1971
- Acrocephalosyndactyly type III: Chotzen's syndromeThe Journal of Pediatrics, 1970
- The Hand and Apertʼs SyndromeJournal of Bone and Joint Surgery, 1970
- Facial asymmetry and abnormalties of palms and ears: A dominantly inherited developmental syndromeThe Journal of Pediatrics, 1970
- Familial Craniosynostosis with Oral AnomaliesDevelopmental Medicine and Child Neurology, 1970
- Dominant erbliche AkrocephalosyndaktylieEuropean Journal of Pediatrics, 1964