Abstract
Von Recklinghausen neurofibromatosis may present many skeletal abnormalities as common features. We describe a family with postaxial polydactyly and neurofibromatosis, an association which has not been previously reported. The special characteristics of postaxial polydactyly of this family were its bilateral and symmetrical appearance, its limitation only to males, simultaneous presence of types A and B in the same patient, and its occurrence in both hands and feet. Postaxial polydactyly type A appeared only in the affected neurofibromatotic members of this family.
Original language | English |
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Pages (from-to) | 202-205 |
Number of pages | 4 |
Journal | Clinical Genetics |
Volume | 32 |
Issue number | 3 |
DOIs | |
State | Published - Sep 1987 |
Keywords
- neonate
- neurofibromatosis
- postaxial polydactyly