A CASE REPORT WITH SEVERE CONGENITAL FACTOR XIII DEFICIENCY AND AN UNCOMPLICATED PREGNANCY AND BIRTH PROCESS
Introduction: Factor XIII deficiency is an extremely rare type among bleeding diathesis. In factor XIII deficiency, normal results of coagulation screening tests are expected. It usually does not cause spontaneous bleeding. Apart from bleeding diathesis, it may cause delayed wound healing and recurr...
Guardado en:
Autores principales: | İbrahim Eker, Yeter Düzenli Kar, Nilgün Eroğlu, Özge Vural, Mehmet Yılmazer |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/d8a9202d20de4f8da740f79a1e7b3a69 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
ACQUIRED FACTOR XIII DEFICIENCY WITH RUNX1 MUTATION, A REPORT OF TWO CASES TREATED WITH FACTOR XIII CONCENTRATE
por: Alfadil Haroon, et al.
Publicado: (2021) -
THE EVALUATION OF CONGENITAL NEUTROPENIA PATIENTS
por: Nihal Karadaş, et al.
Publicado: (2021) -
NEUROBLASTOMA IN A CASE OF CONGENITAL ADRENAL HYPERPLASIA
por: Arzu Yazal Erdem, et al.
Publicado: (2021) -
A RARE CAUSE OF ANEMIA IN ADULTHOOD CONGENITAL DYSERYTHROPETIC ANEMIA
por: Buğra Sağlam, et al.
Publicado: (2021) -
MEDICAL TREATMENT IN HODGKIN LYMPHOMA
por: Nilgun Kurucu
Publicado: (2021)