Congenital longitudinal deficiency of the tibia--report of two cases, both siblings of same parentage
- PMID: 9715119
Congenital longitudinal deficiency of the tibia--report of two cases, both siblings of same parentage
Abstract
Two cases of type IV congenital longitudinal deficiency of the tibia are reported. The patients aged three months and eleven years are siblings of the same parentage, female and male respectively. Autosomal dominance inheritance is the probable mode of inheritance.
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