Fróðskaparrit - 01.01.1965, Qupperneq 105

Fróðskaparrit - 01.01.1965, Qupperneq 105
Dupuytrens Contracture 113 stitutional inherent disease or collagen disease associated with rheumatic disorders. There appears to be no end to the possible aetiological factors which have been discussed by various authors. However there are many aspects for consideration. The condition is prevalent in males. The condition becomes apparent mostly during the middle and latter period of life. It is a condition which may be multicentric in origin and may affect any part of the fascia of the hand, although commoner to the ulnar two fingers. It is a progressive disease. In a number of patients a strong family history has been obtained. Although heredity is thought to be a factor the degree of its importance and its mode of action remains unknown. While the information is suggestive of a familiar factor this does not contribute much to the understanding of the inheri- tance of Dupuytrens contracture. Family History. The family history is summarized in the family pedigree Fig. 1, based on an investigation of all the inhabitants of the islands of Sandoy and Skúvoy (population 31.12.1965: — 1699) and of the parish register for these islands since 1783, 6 succes- sive generations of affected individuals, including males and females suggest autosomal dominant inheritance. The members of the sixth generation below the age of 25 were not included, neither were children of the previous generation who died before they reached the same age. Two (2) of the female members of the second generation 1 and 6 married and left for elsewhere and it was not possible to trace the descendants. On the average in this type of inheritance, one half of the children of the affected parents can be expected to be similarly affected. However, it seems that more than the ex- pected number of the affected family members are found in this pedigree. The finding of unaffected children from affected parents might be considered as evidence of a reduced or low expressivity of the mutant gene which has led to Dupuytrens contracture in others. 9 — Fróðskaparrit 1965
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