Literature DB >> 12687747

Severe protein S deficiency associated with heterozygous factor V Leiden mutation in a child with purpura fulminans.

Yasar Dogan1, Denizmen Aygun, Yelda Yilmaz, Guler Kanra, Gulten Secmeer, Nesrin Besbas, Aytemiz Gurgey.   

Abstract

Homozygous or compound heterozygous protein S (PS) deficiency is very rare in the population; only 8 patients from 6 different families have been reported. On the other hand, the factor V Leiden (FVL) mutation is a frequent cause of inherited prothrombotic disorder. Here the authors report a case of patient with severe PS deficiency associated with the FVL mutation who has had purpura fulminans since the age of 10 days. She is the first child of a consanguineous marriage. Her father is double heterozygous for PS deficiency and FVL mutation and has recurrent thrombosis. This is the first case of severe PS deficiency combined with the FVL mutation. This suggests the need for complete evaluation of patients with purpura fulminans for thrombotic factors.

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Year:  2003        PMID: 12687747

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  2 in total

1.  Late onset thrombosis in a case of severe protein S deficiency due to compound heterozygosity for PROS1 mutations.

Authors:  M J Heeb; S Gandrille; J A Fernandez; J H Griffin; P F Fedullo
Journal:  J Thromb Haemost       Date:  2008-07-01       Impact factor: 5.824

2.  Protein C Deficiency Caused by a Novel Mutation in the PROC Gene in an Infant with Delayed Onset Purpura Fulminans.

Authors:  Mariam S Al Harbi; Ayman W El-Hattab
Journal:  Case Rep Dermatol Med       Date:  2017-09-26
  2 in total

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