-
Hypodysfibrinogenemia, also
termed congenital hypodysfibrinogenemia, is a rare
hereditary fibrinogen disorder cause by
mutations in one or more of the...
- glucocorticoids, and
antileukemic drugs) toxicities.
Congenital hypodysfibrinogenemia is a rare
inherited disorder in
which low
levels (i.e. <150 mg/dl)...
- afibrinogenaemia, hypofibrinogenaemia, dysfibrinogenaemia, and
hypodysfibrinogenemia. Reduced, absent, or
dysfunctional fibrin is
likely to
render patients...
- disorders: afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia, and
hypodysfibrinogenemia.
Congenital afibrinogenemia is
defined as a lack of
fibrinogen in...
-
undetectable due to
mutations in both
fibrinogen genes; b)
congenital hypodysfibrinogenemia, a rare
disorder in
which one or more
genetic mutations cause low...
-
congenital hypodysfibrinogenemia. Both
disorders involve the
circulation of
dysfunctional fibrinogen but in
congenital hypodysfibrinogenemia plasma fibrinogen...
-
Hypodontia dysplasia of
nails Hypodontia of
incisors and
premolars Hypodysfibrinogenemia Hypofibrinogenemia,
familial Hypoglycemia with
deficiency of glycogen...
-
pathological episodes of
bleeding and/or
blood clotting.
Congenital hypodysfibrinogenemia, an
inherited disorder in
which low
levels of
fibrinogen composed...
- to
structurally abnormal fibrinogen viz.,
dysfibrinogenemia and
hypodysfibrinogenemia.
Based on in
vitro studies,
three causes have been hypothesized...
-
several disorders,
including afibrinogenemia, dysfibrinogenemia,
hypodysfibrinogenemia and
thrombotic tendency.
Fibrinogen beta
chain has been
shown to...
