Results 141 to 150 of about 2,267,031 (171)

“Hyper-IgD syndrome” or “mevalonate kinase deficiency”: an old syndrome needing a new name?

Rheumatology International, 2013
We suggest that the use of HIDs name is obsolete, while MKD definition could suit better to the description of the disease.
CELSI, Fulvio, TOMMASINI, ALBERTO, CROVELLA, SERGIO   +2 more
openaire   +3 more sources

[Hyper-IgD syndrome (HIDS)].

Recenti progressi in medicina, 1995
In 1984, Van der Meer first reported six patients with a long history of recurrent attacks of fever of unknown cause and a constantly elevated polyclonal IgD (> 100 U/mL); he suggested the acronym of "hyper-IgD syndrome" (HIDS). A recent literature review identified 60 cases (59 from Europe and 1 from Japan).
openaire   +1 more source

[Periodic fever due to hyper-IgD syndrome].

Nederlands tijdschrift voor geneeskunde, 2000
In a 45-year-old man who from early childhood had been suffering of periodic fever, which did not respond to any therapy attempted, the ultimate diagnosis was hyperimmunoglobulinaemia D syndrome (HIDS). HIDS attacks typically occur every 4-6 weeks and last 3-7 days.
I M, Wauters, R K, Linskens, C D, Stehouwer   +2 more
openaire   +1 more source

Hyper-IgD Syndrome (HIDS)

2021
Homa Seyedmirzaei, Nima Rezaei
openaire   +1 more source

Hyper‐IgD syndrome and hidradenitis suppurativa: An intriguing link

Journal of the European Academy of Dermatology and Venereology, 2023
Laura Calabrese, Antonio Vitale, Chiara Moltrasio, Giovanni Genovese, Maurizio Romagnuolo, Angelo V. Marzano, Roberto Maglie, Pietro Rubegni, Luca Cantarini   +8 more
openaire   +3 more sources

Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.

Nature genetics, 1999
Hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS; MIM 260920) is a rare, apparently monogenic, autosomal recessive disorder characterized by recurrent episodes of fever accompanied with lymphadenopathy, abdominal distress, joint involvement and skin lesions.
J P, Drenth, L, Cuisset, G, Grateau, C, Vasseur, S D, van de Velde-Visser, J G, de Jong, J S, Beckmann, J W, van der Meer, M, Delpech   +8 more
openaire   +1 more source

[Identification of the gene for hyper-IgD syndrome: a model of modern genetics].

Nederlands tijdschrift voor geneeskunde, 2000
Hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS) is a rare autosomal recessive disorder. Patients suffer from recurrent attacks (3-6 days) with fever, abdominal distress, lymphadenopathy, skin lesions and arthralgias. Patients display a constantly elevated serum IgD which serves as a biological marker of the disease. Recently, the gene for
J P, Drenth, H R, Waterham, W, Kuis, S M, Houten, J, Frenkel, R J, Wanders, B T, Poll-The, J W, van der Meer   +7 more
openaire   +1 more source

[The hyper-IgD syndrome].

Deutsche medizinische Wochenschrift (1946), 1996
J P, Drenth, S, Endres, B H, Belohradsky, J W, van der Meer   +3 more
openaire   +1 more source

Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in Hyper-IgD syndrome

Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 2005
Johan Bijzet, Anna Simon, J P H Drenth
exaly  

Syndrome des hyper-IgD et grossesse

La Revue de Médecine Interne, 1998
F Sarrot-Reynauld, C Massot
openaire   +1 more source