| Autor: |
Lerro P; Cattedra di Pediatria, Università degli Studi, Torino., Malorgio E, Oderda G, Perugini L, Dall'Aglio M, Balocco NA |
| Jazyk: |
italština |
| Zdroj: |
Minerva pediatrica [Minerva Pediatr] 1995 Dec; Vol. 47 (12), pp. 541-3. |
| Abstrakt: |
von Willebrand type I disease is an hereditary coagulation disorder characterized by a deficiency of the factor VIII complex: VIII: C, vWF:Ag, vWF:RCoF. The clinical features of this disease are spontaneous bleeding and mucosal or cutaneous bleeding following minimal injuries. The authors describe a case of a 4-year girl with recurrent episodes of gastrointestinal bleeding due to von Willebrand disease. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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