Hyper-IgD and Periodic Fever Syndrome: a New MVK Mutation (p.R277G) Associated...

• Autor(es): Santos, J ; Aróstegui, J ; Brito, MJ ; Neves, C ; Conde, M
• Data: 2014
• Identificador Persistente: http://hdl.handle.net/10400.17/1920
• Origem: Repositório do Centro Hospitalar de Lisboa Central, EPE
• Assunto(s): Hyperimmunoglobulinemia D; Fever; Mevalonate Kinase Deficiency; Phenotype; Child; HDE PED; HDE INF PED; HDE REUM PED
• Tipo de Documento: Artigo
• Idioma: Inglês

Descrição

Hyperimmunoglobulinemia D and periodic fever syndrome (HIDS; MIM#260920) is a rare recessively-inherited autoinflammatory condition caused bymutations in the MVK gene, which encodes for mevalonate kinase, an essential enzyme in the isoprenoid pathway. HIDS is clinically characterized by recurrent episodes of fever and inflammation. Herewe report on the case of a 2 year-old Portuguese boy with recurrent episodes of fever, malaise, massive cervical lymphadenopathy and hepatosplenomegaly since the age of 12 months. Rash, arthralgia, abdominal pain and diarrhea were also seen occasionally. During attacks a vigorous acute-phase response was detected, including elevated erythrocyte sedimentation rate, C-reactive protein, serum amyloid A and leukocytosis. Clinical and laboratory improvement was seen between attacks. Despite normal serum IgD level, HIDS was clinically suspected. Mutational MVK analysis revealed the homozygous genotype with the novel p.Arg277Gly (p.R277G) mutation, while the healthy non consanguineous parents were heterozygous. Short nonsteroidal anti-inflammatory drugs and corticosteroid courses were given during attacks with poor benefits, where as anakinra showed positive responses only at high doses. The p.R277Gmutation here described is a novel missense MVK mutation, and it has been detected in this casewith a severe HIDS phenotype. Further studies are needed to evaluate a co-relation genotype, enzyme activity and phenotype, and to define the best therapeutic strategies.