Abstract
A clinical and laboratory investigation of a kindred in which haemophilia A and autosomal recessive von Willebrand's disease (VWD) were concomitantly present is described. 3 male patients were shown to be hemizygotes for moderate haemophilia A, one female appeared to be haemophilia A carrier and 3 males showed laboratory findings consistent with heterozygosity for autosomal recessive VWD. In one woman, the pedigree and laboratory findings suggest the possibility of double heterozygosity.
| Original language | English |
|---|---|
| Pages (from-to) | 423-428 |
| Number of pages | 6 |
| Journal | Scandinavian Journal of Haematology |
| Volume | 20 |
| Issue number | 5 |
| Publication status | Published - 1978 |
Fingerprint
ASJC Scopus subject areas
- Hematology
Cite this
Coexistence of haemophilia A and Von Willebrand's disease in the same kindred. / Gastaldi, G.; Rasore-Quartino, A.; Galletti, A.; Campanella, A.; Barone, E.; Mannucci, P. M.
In: Scandinavian Journal of Haematology, Vol. 20, No. 5, 1978, p. 423-428.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Coexistence of haemophilia A and Von Willebrand's disease in the same kindred
AU - Gastaldi, G.
AU - Rasore-Quartino, A.
AU - Galletti, A.
AU - Campanella, A.
AU - Barone, E.
AU - Mannucci, P. M.
PY - 1978
Y1 - 1978
N2 - A clinical and laboratory investigation of a kindred in which haemophilia A and autosomal recessive von Willebrand's disease (VWD) were concomitantly present is described. 3 male patients were shown to be hemizygotes for moderate haemophilia A, one female appeared to be haemophilia A carrier and 3 males showed laboratory findings consistent with heterozygosity for autosomal recessive VWD. In one woman, the pedigree and laboratory findings suggest the possibility of double heterozygosity.
AB - A clinical and laboratory investigation of a kindred in which haemophilia A and autosomal recessive von Willebrand's disease (VWD) were concomitantly present is described. 3 male patients were shown to be hemizygotes for moderate haemophilia A, one female appeared to be haemophilia A carrier and 3 males showed laboratory findings consistent with heterozygosity for autosomal recessive VWD. In one woman, the pedigree and laboratory findings suggest the possibility of double heterozygosity.
UR - http://www.scopus.com/inward/record.url?scp=0017863444&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0017863444&partnerID=8YFLogxK
M3 - Article
C2 - 307271
AN - SCOPUS:0017863444
VL - 20
SP - 423
EP - 428
JO - European Journal of Haematology
JF - European Journal of Haematology
SN - 0902-4441
IS - 5
ER -