Fig. 3From: Alpha 2-antiplasmin deficiency in a Sudanese child: a case reportAutosomal recessive trait pedigree of the Sudanese male patient with α2-AP deficiency. Each subject can be located in the pedigree by a Roman numeral indicating generation. The patient (II 2) possessing 0.2 IU/ml α2-AP in plasma was believed to be a heterozygoteBack to article page