Results 191 to 200 of about 7,350 (240)
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Mucocutaneous lymph node syndrome (Kawasaki disease)

Oral Surgery, Oral Medicine, Oral Pathology, 1989
Mucocutaneous lymph node syndrome has rarely been reported in the dental literature despite the orofacial features characteristic of the disease. A case is reported in which the cardinal signs were present: erythema of the oral mucosa, cervical lymphadenopathy, conjunctivitis, pyrexia, and desquamation of the skin of the hands and feet.
Ogden, G. R., Kerr, M.
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Acute Febrile Mucocutaneous Lymph Node Syndrome

Archives of Pediatrics & Adolescent Medicine, 1980
More than a decade ago, Tomisaku Kawasaki, a Japanese pediatrician, described an acute exanthematous disease characterized by persistent fever, mucous membrane hyperemia, cervical lymph node enlargement, and periungal desquamation in 50 infants and children who had been seen during the preceding six-year period at the Japan Red Cross Medical Center in ...
R, Yanagihara, J K, Todd
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Mucocutaneous Lymph Node Syndrome in Arizona

Archives of Pediatrics & Adolescent Medicine, 1976
Mucocutaneous lymph node syndrome (MLNS) is a newly recognized entity, widely prevalent in Japan. It has also been reported in Korea, Hawaii, and Greece. We have recently seen four white children, 3 to 4 1/2 years of age, with MLNS, in Tucson, Ariz. They had all the principal signs and symptoms characteristic of MLNS.
T J, John, C D, DeBenedetti, M L, Zee
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Mucocutaneous Lymph Node Syndrome in Denver

Archives of Pediatrics & Adolescent Medicine, 1976
Four children with acute febrile mucocutaneous lymph node syndrome (MLNS) were hospitalized in Denver over a two-year period. The children had most of the principle features of this recently described syndrome, including prolonged fever unresponsive to antibiotics, an erythematous rash, conjunctivitis, pharyngitis, and nonsuppurative cervical ...
B A, Lauer   +3 more
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Mucocutaneous lymph node syndrome.

IMJ. Illinois medical journal, 1978
Mucocutaneous lymph node syndrome (MLNS) is a recently described disease entity of unknown etiology that mainly affects children. The disease is characterized by fever, oral mucosal changes, cervical lymphadenopathy and a peripheral skin rash with induration of hands and feet and subsequent desquamation.
M, Miriovsky, J S, Downing
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Mucocutaneous lymph node syndrome with necrotic pharyngitis

European Journal of Pediatrics, 1980
We report a case of Kawasaki disease in which some unusual symptoms, including petechiae, an urticaria-like eruption, and necrotic pharyngitis, made the diagnosis difficult. No complications were detected during a follow-up period of 15 months.
Brion, Luc   +6 more
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HLA Antigens in Mucocutaneous Lymph Node Syndrome

Archives of Pediatrics & Adolescent Medicine, 1977
Kawasaki disease or mucocutaneous lymph node syndrome (MLNS), first described by Kawasaki 1-2 in 1974, is an acute febrile disease of unknown etiology. Until recently, more than 6,000 cases of this disease have been listed in the survey of a special study group supported by the Japanese Ministry of Health and Welfare.
I, Matsuda   +4 more
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Mucocutaneous lymph node syndrome with testicular involvement

Irish Journal of Medical Science, 1980
A case of mucocutaneous lymph-node syndrome (MLNS) occurring in a 6 year old boy is reported. This is the first case we are aware of in which epididymo-orchitis is described.
K D, Connolly, D, Timmons
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Mucocutaneous Lymph Node Syndrome: Second Alert

JAMA: The Journal of the American Medical Association, 1977
An earlier JAMA editorial 1 described the symptoms and course of mucocutaneous lymph node syndrome (MLNS), which is evidently a new disease or a mysterious variant of some other known disease. The editorial mentioned that what was formerly a "Japanese" disease affecting young children had been identified in widely separated areas of the United States ...
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