Search results
Results from the WOW.Com Content Network
The symptoms of DRESS syndrome usually begin 2 to 6 weeks but uncommonly up to 8–16 weeks after exposure to an offending drug. Symptoms generally include fever, an often itchy rash which may be morbilliform or consist mainly of macules or plaques, facial edema (i.e. swelling, which is a hallmark of the disease), enlarged and sometimes painful lymph nodes, and other symptoms due to ...
The DRESS syndrome is a Type IV, Subtype IVb, hypersensitivity drug reaction, i.e. a reaction dependent on CD4(+) cells and the cell- and tissue-injuring action of eosinophils. [ 2 ] [ 8 ] Skin lesions inflict 73% to 100% of afflicted individuals; they are generally infiltrative macules and plaques .
Allopurinol hypersensitivity syndrome (AHS) typically occurs in persons with preexisting kidney failure. [3]: 119 Weeks to months after allopurinol is begun, the patient develops a morbilliform eruption [3]: 119 or, less commonly, develops one of the far more serious and potentially lethal severe cutaneous adverse reactions viz., the DRESS syndrome, Stevens Johnson syndrome, or toxic epidermal ...
Microphthalmia–dermal aplasia–sclerocornea syndrome; Middle cerebral artery syndrome; Middle child syndrome; Middle East respiratory syndrome; Mikulicz syndrome; Mild androgen insensitivity syndrome; Milk-alkali syndrome; Millard–Gubler syndrome; Miller Fisher syndrome; Miller syndrome; Miller–Dieker syndrome; Milroy's disease ...
Stevens–Johnson syndrome (SJS) is a type of severe skin reaction. [1] Together with toxic epidermal necrolysis (TEN) and Stevens–Johnson/toxic epidermal necrolysis (SJS/TEN) overlap, they are considered febrile mucocutaneous drug reactions and probably part of the same spectrum of disease, with SJS being less severe.
Peeling skin syndrome (acral peeling skin syndrome, continual peeling skin syndrome, familial continual skin peeling, idiopathic deciduous skin, keratolysis exfoliativa congenita) Pfeiffer syndrome; Photosensitivity–ichthyosis–brittle sulfur-deficient hair–impaired intelligence–decreased fertility–short stature syndrome
The earliest recorded case of CHILD syndrome was in 1903. Otto Sachs was accredited for first describing the clinical characteristics of the syndrome in an 8-year-old girl. The nearest proceeding news on the topic was a report in 1948 by Zellweger and Uelinger, who reported a patient with "half-sided osteochondrodermatitis and nevus ...
A syndrome is a set of medical signs and symptoms which are correlated with each other and often associated with a particular disease or disorder. [1] The word derives from the Greek σύνδρομον, meaning "concurrence". [2]: 1818 When a syndrome is paired with a definite cause this becomes a disease. [3]