De novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome
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DOI: 10.1016/j.ymgmr.2018.06.001
Abstract: Complex phenotypes may represent novel syndromes that are the composite interaction of several genetic and environmental factors. We describe an 9-year old male with high functioning autism spectrum disorder and Muckle-Wells syndrome who at age… read more here.
Keywords: wells syndrome; fatigue somnolence; nlrp3 mutations; muckle wells ... See more keywords
Rare presentation of Wells syndrome mimicking angioedema: a case report
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DOI: 10.1684/ejd.2022.4282
Abstract: 411 Figure 1. Clinical and histopathological features of the patient. A) Solitary, ill-defined erythema on the left cheek five years ago. B) Newly occurring erythema with a previous biopsy scar. C) Haematoxylin-eosin staining of the… read more here.
Keywords: presentation wells; angioedema case; mimicking angioedema; wells syndrome ... See more keywords
Allergic contact stomatitis caused by (meth)acrylates following sensitization by artificial nails, 20 years previously
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DOI: 10.1684/ejd.2022.4284
Abstract: 413 (1 mg/kg daily for a week) along with topical corticosteroids with good response. The lip was treated with intralesional corticosteroids (figure 1G). The aetiology of Wells syndrome is unknown. It is thought that an… read more here.
Keywords: topical corticosteroids; stomatitis caused; contact stomatitis; wells syndrome ... See more keywords
Erratum: Muckle–Wells syndrome in an Indian family associated with NLRP3 mutation
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DOI: 10.4103/0022-3859.169506
Abstract: [This corrects the article DOI: 10.4103/0022-3859.153107]. read more here.
Keywords: indian family; erratum muckle; wells syndrome; syndrome indian ... See more keywords