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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]
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.
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.
It encompasses a spectrum of three clinically overlapping autoinflammatory syndromes including familial cold autoinflammatory syndrome (FCAS, formerly termed familial cold-induced urticaria), the Muckle–Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease (NOMID, also called chronic infantile neurologic cutaneous and ...
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 ...
Weil's disease (/ ˈ v aɪ l z / VILES), [12] the acute, severe form of leptospirosis, causes the infected individual to become jaundiced (skin and eyes become yellow), develop kidney failure, and bleed. [6] Bleeding from the lungs associated with leptospirosis is known as severe pulmonary haemorrhage syndrome. [5]
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 ...
Hay–Wells syndrome (AEC syndrome, ankyloblepharon filiforme adnatum–ectodermal dysplasia–cleft palate syndrome, ankyloblepharon–ectodermal defects–cleft lip and palate syndrome, ankyloblepharon–ectodermal dysplasia–clefting syndrome)