Results 151 to 160 of about 5,132 (186)

A patient with hyper-IgD syndrome responding to anti-TNF treatment

Clinical Rheumatology, 2006
The hyperimmunoglobulinemia D periodic fever syndrome (HIDS) is caused by recessive mutations in the mevalonate kinase gene, which encodes an enzyme involved in cholesterol and nonsterol isoprenoid biosynthesis. The pathogenesis and treatment remains unclear. We describe a 6-year-old Turkish girl with severe disease.
Demirkaya, Erkan, Caglar, M. Kazim, Waterham, Hans R., Topaloglu, Rezan, Ozen, Seza   +4 more
openaire   +3 more sources

Hyper-IgD syndrome and familial Hibernian fever are true periodic fever syndromes

The Journal of Pediatrics, 2000
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Drenth, J.P.H., Powell, R.J.
openaire   +2 more sources

A case series of three patients with hyper IgD syndrome

Journal of Allergy and Clinical Immunology, 2004
Abstract Rationale This case series brings to light three newly diagnosed cases of Hyper IgD Syndrome (HIDS), a rare inherited periodic fever with only 193 reported cases world-wide through May 2003. Methods Three patients were diagnosed with HIDS and their clinical and laboratory data are presented.
Y. Padeh, A. Rubinstein
openaire   +1 more source

“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We suggest that the use of HIDs name is obsolete, while MKD definition could suit better to the description of the disease.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

[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)].

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

Hyper-IgD syndrome

1996
K.U.
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

Hyper-IgD Syndrome (HIDS)

2021
Homa Seyedmirzaei, Nima Rezaei
openaire   +1 more source

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