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Eosinophilic cellulitis, also known as Wells' syndrome (not to be confused with Weil's disease), is a skin disease that presents with painful, red, raised, and warm patches of skin. [2] The rash comes on suddenly, lasts for a few weeks, and often repeatedly comes back. [2] Scar formation does not typically occur. [1]
Hay–Wells syndrome (also known as AEC syndrome; see Naming) is one of at least 150 known types of ectodermal dysplasia. [ 1 ] [ 2 ] These disorders affect tissues that arise from the ectodermal germ layer , such as skin, hair, and nails.
Muckle–Wells syndrome (MWS) 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.
The syndromes within CAPS overlap clinically, and patients may have features of more than one disorder. In a retrospective cohort of 136 CAPS patients with systemic involvement from 16 countries, [2] the most prevalent clinical features were fever (84% of cases, often with concurrent constitutional symptoms such as fatigue, malaise, mood disorders or failure to thrive), skin rash (either ...
Mowat–Wilson syndrome; Moyamoya disease; Moynahan syndrome; Muckle–Wells syndrome; Muenke syndrome; Muir–Torre syndrome; Mukamel syndrome; Multiple endocrine neoplasia type 1; Multiple endocrine neoplasia type 2; Multiple evanescent white dot syndrome; Multiple hamartoma syndrome; Multiple organ dysfunction syndrome; Multiple pterygium ...
Wilkie–Taylor–Scambler syndrome; Willebrand disease, acquired; Willebrand disease; Willems–De vries syndrome; Williams syndrome; Wilms' tumor; Wilms tumor and pseudohermaphroditism; Wilms tumor radial bilateral aplasia; Wilms tumor-aniridia syndrome; Wilson's disease; Wilson–Turner syndrome; Winchester syndrome; Winkelman–Bethge ...
Chronic granulomatous disease (Bridges–Good syndrome, chronic granulomatous disorder, Quie syndrome) Common variable immunodeficiency (acquired hypogammaglobulinemia) Complement deficiency; DiGeorge syndrome (DiGeorge anomaly, thymic hypoplasia) Graft-versus-host disease; Griscelli syndrome; Hyper-IgE syndrome (Buckley syndrome, Job syndrome)
Wells-Jankovic syndrome is a rare neurologic disorder characterized by spastic paraparesis presents in late childhood along with hearing loss. [2] In 1986 Wells and Jankovic reported the condition in 6 males. [3] There have been no new cases in the literature since 1986. [2]