| 词条 | Muckle–Wells syndrome |
| 释义 |
| name = Muckle–Wells syndrome | synonyms = | image = Autosomal dominant - en.svg | caption = This condition is inherited in an autosomal dominant manner | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} Muckle–Wells syndrome (MWS), also known as urticaria-deafness-amyloidosis syndrome (UDA),[1] is a rare autosomal dominant disease which causes sensorineural deafness and recurrent hives, and can lead to amyloidosis. Individuals with MWS often have episodic fever, chills, and joint pain. As a result, MWS is considered a type of periodic fever syndrome. MWS is caused by a defect in the CIAS1 gene which creates the protein cryopyrin. MWS is closely related to two other syndromes, familial cold urticaria and neonatal onset multisystem inflammatory disease—in fact, all three are related to mutations in the same gene and subsumed under the term cryopyrin-associated periodic syndromes (CAPS). Sign and symptoms
CausesMWS occurs when a mutation in the CIAS1 gene, encoding for NLRP3, leads to increased activity of the protein cryopyrin. This protein is partly responsible for the body's response to damage or infection. During these states, a cytokine called interleukin 1β is produced by an innate immune cell known as a macrophage. This cytokine interacts with a receptor on the surface of other immune cells to produce symptoms of inflammation such as fever, arthritis, and malaise. In MWS, the increased activity of cryopyrin leads to an increase in interleukin 1β. This leads to inflammation all throughout the body with the associated symptoms.[2] Diagnosis{{Empty section|date=January 2017}}Treatment
PrognosisThe chronic inflammation present in MWS over time can lead to deafness. In addition, the prolonged inflammation can lead to deposition of proteins in the kidney, a condition known as amyloidosis. HistoryMWS was first described in 1962 by Thomas James Muckle (1938-2014)[4] and Michael Vernon Wells (born 1932).[5] Society and cultureThe CBC Radio One program, White Coat, Black Art, hosted by Dr. Brian Goldman, presents a real-life study of the self-diagnosis by and successful treatment of a father and daughter with Muckle–Wells syndrome: 24 September 2016 episode In the episode of popular TV series House, the main patient of the Season 7 episode Recession Proof is ultimately diagnosed with this condition.{{citation needed|date=January 2017}}In an episode of TV series Cake Boss, Buddy Valastro works with a girl with this condition through Make-A-Wish Foundation. See also
References1. ^ORPHANET - About rare diseases - About orphan drugs 2. ^{{cite journal | pmid = 16407890 |name-list-format=vanc| last1 = Mariathasan | first1 = S| doi=10.1038/nature04515 | last2 = Weiss | first2 = DS | last3 = Newton | first3 = K | last4 = McBride | first4 = J | last5 = O'Rourke | first5 = K | last6 = Roose-Girma | first6 = M | last7 = Lee | first7 = WP | last8 = Weinrauch | first8 = Y | last9 = Monack | first9 = DM | last10 =Dixit | first10 =Vishva M. | title = Cryopyrin activates the inflammasome in response to toxins and ATP | journal = Nature | volume=440 | issue=7081 | pages = 228–32 |date=March 2006| display-authors =8 }} 3. ^{{cite journal | pmid = 16531551 |name-list-format=vanc| last1 = Rynne | pmc = 1798106 | first1 = M| doi=10.1136/ard.2005.038091 | last2 = MacLean | first2 = C | last3 = Bybee | first3 = A | last4 = McDermott | first4 = MF | last5 = Emery | first5 = P | title = Hearing improvement in a patient with variant Muckle‐Wells syndrome in response to interleukin 1 receptor antagonism | journal = Annals of the Rheumatic Diseases | volume=65 | issue=4 | pages = 533–4 |date=April 2006}} 4. ^{{cite news|last1=Churchill|first1=Dave|title=Former McMaster professor had taste for adventure and great wine|url=http://www.thespec.com/news-story/5206266-former-mcmaster-professor-had-taste-for-adventure-and-great-wine/|publisher=Hamilton Spectator}} 5. ^{{cite journal | pmid = 14476827 | last1 = Muckle |name-list-format=vanc| first1 = TJ | title = Urticaria, deafness, and amyloidosis: a new heredo-familial syndrome | journal = The Quarterly Journal of Medicine| volume=31 | pages = 235–48 |date=April 1962}} External links{{Medical resources| DiseasesDB = 30159 | ICD10 = {{ICD10|E|85|0|e|75}}, {{ICD10|L|50|8|l|50}} | ICD9 = | ICDO = | OMIM = 191900 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = D056587 | Orphanet = 575 }}
6 : Rheumatology|Autoinflammatory syndromes|Rare syndromes|Genetic syndromes|Syndromes with sensorineural hearing loss|Syndromes affecting the skin |
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