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Zespół hiper-IgD (ang. hyper-IgD syndrome, HIDS). [W : zespoły autozapalne]

, 2018
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A patient with hyper-IgD syndrome in Antalya, Turkey

Clinical Rheumatology, 2004
Hyper-IgD syndrome is a periodic fever syndrome that presents with recurrent episodes of high fever accompanied by lymphadenopathy, abdominal distress, arthralgias or arthritis, headache and skin lesions. The diagnosis is based on clinical grounds and elevated serum IgD levels (>100 U/ml), but requires a high index of suspicion, and a mevalonate kinase
Erkan, Coban, Ender, Terzioğlu
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Hyper-IGD syndrome: A new case treated with colchicine

Clinical Rheumatology, 1988
We report a new case of hyper-IgD syndrome, a recently described disease characterized by recurrent episodes of fever with headache, bilateral cervical lymphadenopathy and, more rarely, abdominal pain and diarrhoea. Polyclonal increase of serum IgD is the most important laboratory finding.
P A, Ostuni, P, Lazzarin, G, Ongaro, R, Gusi, S, Todesco, P F, Gambari   +5 more
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Das Hyper-IgD-Syndrom (The hyper-IgD-syndrome)

Zeitschrift f�r Rheumatologie, 1997
We report on a 6-year-old Romanian girl with recently diagnosed hyper-IgD-syndrome. The leading symptom of this rare disease are periodic pyrexia, joint involvements (arthralgias/arthritis) and swollen lymph nodes. A permanent increase of alpha 1-acid glycoprotein fucosylation indicates persisting inflammation.
J. Suschke, J.-U. Walther
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Crescentic glomerulonephritis in hyper IgD syndrome

Pediatric Nephrology, 1999
The hyperimmunoglobulinemia D syndrome (HIDS) is a well-defined entity resembling familial Mediterranean fever. HIDS is a systemic inflammatory disease associated with stimulation of T-cell-mediated immunity. These patients are at low risk for amyloidosis and are not known to develop nephropathy.
M, Tsimaratos, I, Koné-Paut, L, Daniel, M C, Gubler, B, Dussol, G, Picon   +5 more
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Hyper-IgD syndrome or mevalonate kinase deficiency

Current Opinion in Rheumatology, 2011
The hyper-IgD and periodic fever syndrome (HIDS) is one of the classical monogenetic hereditary autoinflammatory disorders, and together with the more severe mevalonic aciduria it is also known as 'mevalonate kinase deficiency' (MKD). In this study, we will give an overview of the primary research on mevalonate kinase deficiency published in the past 2
Stoffels, M., Simon, A.
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Un cas de syndrome hyper-IgD

Revue Francophone des Laboratoires, 2019
Resume Les fievres recurrentes de l’enfant sont de diagnostic etiologique difficile, car concernent des anomalies metaboliques ou genetiques souvent non encore connues. Elles sont associees a des maladies dont les mecanismes physiopathologiques, et donc les marqueurs biologiques, commencent a etre elucides.
Anaïs Nombel, Marie-Nathalie Kolopp-Sarda   +1 more
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Treatment of adult hyper-IgD syndrome with canakinumab

The Journal of Allergy and Clinical Immunology: In Practice, 2015
Hyper-IgD and periodic fever syndrome (HIDS) is a rare, autosomal-recessive autoinflammatory disease characterized by lifelong recurrent episodes of systemic inflammation. HIDS frequently presents in infancy with intermittent fevers lasting from 4 to 7 days, recurring every 4 to 6 weeks.
Casey D, Curtis, Charity C, Fox
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Hyper-IgD syndrome with novel mutation in a Japanese girl

Modern Rheumatology, 2008
Hyperimmunoglobulin D and periodic fever syndrome (HIDS) is an autosomal recessive auto-inflammatory disorder characterized by recurrent febrile attacks with lymphadenopathy, abdominal distress, skin eruptions and joint involvement. We discuss the case of a 15-year-old Japanese girl who had presented with periodic fever, hepatosplenomegaly and ...
Takuya, Naruto, Yasuo, Nakagishi, Masaaki, Mori, Takako, Miyamae, Tomoyuki, Imagawa, Shumpei, Yokota   +5 more
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A patient with hyper-IgD syndrome responding to simvastatin treatment

European Journal of Internal Medicine, 2008
The hyper-IgD syndrome (HIDS) is an autosomal recessively inherited auto-inflammatory syndrome, caused by deficient enzyme activity of mevalonate kinase (MVK), an enzyme in the isoprenoid pathway. Patients present with a long history of recurrent fever attacks, accompanied by abdominal pain, skin lesions, lymphadenopathy and arthralgia.
H, Attout, S, Guez, I, Ranaivo, N, Jameerbaccus, C, Series   +4 more
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