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Article in English | IMSEAR | ID: sea-80565

ABSTRACT

Congenital extremity anomalies have many modes of presentation. Interruption of vascular supply with thrombophily is a rare cause of congenital extremity absence. Here it is presented a 7 mth old male with absence of the left lower extremity. Laboratory tests revealed Factor V Leiden and Prothrombin G20210A heterozygote mutation and that was as the cause of extremity absence. At the patients with congenital extremity absences, it is not imprudent to explore a possible thrombophilic mutation along with other known etiologic factors.


Subject(s)
Diseases in Twins , Factor V/genetics , Foot Deformities, Congenital/etiology , Humans , Infant , Leg/abnormalities , Male , Point Mutation , Thrombosis/complications
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