Results 281 to 290 of about 78,624 (321)
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New England Journal of Medicine, 1973
Pure red cell aplasia (PRCA) was first described by Kaznelson (1922) as an anemia due to an almost complete cessation of erythropoiesis, but without leukopenia or thrombocytopenia. This condition usually can be clearly distinguished from aplastic anemia in which low blood white cell and platelet concentrations accompany the anemia (Van Der Weyden and ...
Howard L. Bleich +2 more
openaire +2 more sources
Pure red cell aplasia (PRCA) was first described by Kaznelson (1922) as an anemia due to an almost complete cessation of erythropoiesis, but without leukopenia or thrombocytopenia. This condition usually can be clearly distinguished from aplastic anemia in which low blood white cell and platelet concentrations accompany the anemia (Van Der Weyden and ...
Howard L. Bleich +2 more
openaire +2 more sources
Aplasia cutis congenita with dystrophic epidermolysis bullosa: clinical and mutational study
British Journal of Dermatology, 2014Aplasia cutis congenita (ACC) has been associated with all clinical forms of inherited epidermolysis bullosa (EB), including dominant and recessive dystrophic EB (DDEB and RDEB).
C. Chiaverini +16 more
semanticscholar +1 more source
Ugeskrift for laeger, 2015
Aplasia cutis congenita (ACC) is a rare congenital defect of the skin, with an estimated incidence of 1:3,000-10,000 births. We report three cases of non-syndromic ACC, of which one was not acknowledged immediately after birth. All the patients were treated conservatively or with standard wound/encephalocele treatment with satisfying results.
Rogvi, Rasmus +2 more
openaire +2 more sources
Aplasia cutis congenita (ACC) is a rare congenital defect of the skin, with an estimated incidence of 1:3,000-10,000 births. We report three cases of non-syndromic ACC, of which one was not acknowledged immediately after birth. All the patients were treated conservatively or with standard wound/encephalocele treatment with satisfying results.
Rogvi, Rasmus +2 more
openaire +2 more sources