T. Dyke et al., HEMOPHILIA-A IN THE HIGHLANDS - THE INVESTIGATION AND MANAGEMENT OF 2FAMILIES IN TARI, Papua New Guinea medical journal, 36(1), 1993, pp. 22-28
A 12-year-old boy from Tari in the Southern Highlands of Papua New Gui
nea presented with prolonged bleeding from a minor injury to the lip.
He had a history of profuse bleeding and joint swelling following mino
r trauma. He has two younger brothers with a similar history. It was d
emonstrated that they had a coagulation profile compatible with factor
VIII deficiency and a family tree suggestive of haemophilia A. A furt
her case was investigated some months later. Despite the neighbouring
places of residence of the two families no familial connection could b
e established by involved discussions between family members. This was
confirmed by reviewing the data held on the demographic surveillance
system of the Tari Unit of the Papua New Guinea Institute of Medical R
esearch. These families are considered against a background of the dia
gnosis and management of this condition in a rural part of Papua New G
uinea. The long-term support of these patients and other similarly aff
ected individuals presents difficult clinical and ethical problems for
rural health services.