Fanconi’s Anemia:
Pacific Journal of Medical Sciences
; : 66-70, 2018.
Article
ي En
| WPRIM
| ID: wpr-972890
المكتبة المسؤولة:
WPRO
ABSTRACT
@#Fanconi’s Anemia (FA) is a rare autosomal recessive disorder characterized by thrombocytopenia,diverse congenital malformations which include skeletal malformations, hyperpigmentation, urogenital, renal and cardiac anomalies. We report a case of Fanconi anemia who presented with thrombocytopenia, bilateral hypoplastic thumbs, café-au-lait spots, with severe bleeding from the gingiva managed with platelet transfusion and extraction of the tooth was done
النص الكامل:
1
الفهرس:
WPRIM
اللغة:
En
مجلة:
Pacific Journal of Medical Sciences
السنة:
2018
نوع:
Article