Annals of Clinical Biochemistry > Volume 45, Number 6 > Pp. 610-611

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Acute intermittent porphyria presenting with a subarachnoid haemorrhage

Charles van Heyningen¹ and David M Simms²

¹ Clinical Laboratories, University Hospital Aintree, Liverpool L9 7AL; ² Chemical Pathology Department, Kingston Hospital, Kingston upon Thames KT2 7QB, UK

View larger version (5K): [in this window] [in a new window]   Figure 1 Pedigree showing autosomal dominant transmission of acute intermittent porphyria due to a R173W gene mutation. In the second generation, the deceased proband had five unaffected brothers, two unaffected sisters and one affected sister

 

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