-transparent.png){kind=logo}
We are treating successfully for seven years a nineteenyear-old girl with Fanconi's aplastic anemia combining androgenes and corticosteroids. The cytogenetic analyses of the other family members showed typical chromosome abnormalities in her father, mother and a twelve-year old sister. In the bone marrow of this sister there are already present the first morphological abnormalities, although the values of her peripheral blood counts are still normal. In the present paper we are discussing when to start the specific therapy in the affected sister.
Related Publications
N Mihevc, and
M Benedik, and
D Blatnik
April 1991,
Seminars in hematology,
N Mihevc, and
M Benedik, and
D Blatnik
September 1974,
Srpski arhiv za celokupno lekarstvo,
N Mihevc, and
M Benedik, and
D Blatnik
April 1965,
Dapim refuiim. Folia medica,
N Mihevc, and
M Benedik, and
D Blatnik
August 1961,
Archivos de pediatria del Uruguay,
N Mihevc, and
M Benedik, and
D Blatnik
August 1972,
Wiadomosci lekarskie (Warsaw, Poland : 1960),
N Mihevc, and
M Benedik, and
D Blatnik
January 1989,
Bailliere's clinical haematology,
N Mihevc, and
M Benedik, and
D Blatnik
January 1977,
Bilten za hematologiju i transfuziju,
N Mihevc, and
M Benedik, and
D Blatnik
July 1999,
Indian pediatrics,
N Mihevc, and
M Benedik, and
D Blatnik
June 1983,
American journal of medical genetics,
