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Sweet syndrome (SS), or acute febrile neutrophilic dermatosis, [1] [2] is a skin disease characterized by the sudden onset of fever, an elevated white blood cell count, and tender, red, well-demarcated papules and plaques that show dense infiltrates by neutrophil granulocytes on histologic examination.
Sweet's syndrome-like dermatosis is a cutaneous condition associated with bowel disorders. [1] See also. Sweet's syndrome; List of cutaneous conditions; References
Supernumerary nipples–uropathies–Becker's nevus syndrome; Supernumerary phantom limb; Survivor syndrome; Susac's syndrome; Sweet's syndrome; Swyer–James syndrome; Syndrome of inappropriate antidiuretic hormone secretion; Syndrome of subjective doubles; Syndrome Without A Name; HHH syndrome; Systemic inflammatory response syndrome; Sézary ...
Reactive neutrophilic dermatoses are a spectrum of conditions mediated by neutrophils, and typically associated with underlying diseases, such as inflammatory bowel disease and hematologic malignancy.
The skin can be involved in the form of leukemia cutis; Sweet's syndrome; or non-specific findings: flat lesions , raised lesion papules, pyoderma gangrenosum and vasculitis. [ 8 ] Some people with AML may experience swelling of the gums because of infiltration of leukemic cells into the gum tissue. [ 7 ]
LPIN2, D18S60. Synonyms: Majeed syndrome. Complement component 2 deficiency: Possibly symptomatic of autoimmune diseases, but not a disease. Congenital heart block: May be related to autoimmune activity in the mother. Contact dermatitis: A hypersensitivity. Cushing's syndrome: No consistent evidence of association with autoimmunity.
Smith-Kingsmore syndrome is a rare genetic disorder that is caused by gain-of-function mutation in a gene MTOR. The facial features of this syndrome are triangular face with a pointed chin, frontal bossing , hypertelorism , eyes with downslanting palpebral fissures , a flat nasal bridge , a long philtrum .
Saal Bulas syndrome; Saal Greenstein syndrome; Sabinas brittle hair syndrome; Saccharopinuria; Sackey–Sakati–Aur syndrome; Sacral agenesis; Sacral defect anterior sacral meningocele