Results 141 to 150 of about 2,294 (167)

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

Overlap of Familial Mediterranean Fever and Hyper-IgD Syndrome in an Arabic Kindred

Journal of Clinical Immunology, 2015
Hyperimmunoglobulinemia D Syndrome (HIDS) has rarely been reported in Arabs. Moreover, the simultaneous presence of mutations in MEFV and MVK segregating in the same family is exceptional. We report an Arabic girl presenting since the age of 8-years with two patterns of recurrent episodes of fever, and associated with a spectrum of clinical features ...
Taha, Moussa, Buthaina, Aladbe, Rowaida Z, Taha, Elaine F, Remmers, Hatem, El-Shanti, Basil M, Fathalla   +5 more
openaire   +2 more sources

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We suggest that the use of HIDs name is obsolete, while MKD definition could suit better to the description of the disease.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

Recurrent pericarditis in hyper-IgD syndrome

, 2009
Breda L, Nozzi M, Di Marzio D, De Sanctis S, Gattorno M, CHIARELLI, Francesco   +5 more
openaire   +2 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 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

[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

[Hyper IgD syndrome].

Annales de dermatologie et de venereologie, 1998
F, Aubin, P, Humbert
openaire   +1 more source

Hyper-IgD syndrome with novel mutation in a Japanese girl

Modern Rheumatology, 2009
Masaaki Mori, Tomoyuki Imagawa, Naruto Takuya   +2 more
exaly