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Mucocutaneous lymph node syndrome: A new clinical entity

open access: closedThe Laryngoscope, 1977
AbstractA six‐year‐old black male presented to the Otolaryngology service with fever, sore throat and an inflammatory mass in the left neck. Forty‐eight hours later he developed the full blown clinical picture of mucocutaneous lymph node syndrome (MLNS).
Charles W. Gross, Morrow Chamberlain
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Complement and protease inhibitors in the mucocutaneous lymph node syndrome

European Journal of Pediatrics, 1983
Total hemolytic activity of serum (CH50), complement components C3 and C4, alpha 1antitrypsin (alpha 1AT), alpha 1antichymotrypsin (alpha 1X), antithrombin III (AT III), alpha 2 macroglobulin (alpha 2M), and inter-alpha-inhibitor (I-alpha-I) were measured in 23 Japanese and 19 European children with the Mucocutaneous Lymph node Syndrome (MCLS) during ...
T. Kawasaki   +3 more
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Mucocutaneous lymph node syndrome in the continental United States

open access: closedThe Journal of Pediatrics, 1976
mercury that persisted (Table II) even after the blood mercury level decreased from 456/~g/dl to 15/~g/dl. The persistently high tissue levels of mercury obviously could have contributed to the deterioration and death of this patient despite the important fall in the concentrat ion o f blood mercury. The underlying congenital heart disease and possible,
James S. Brown   +5 more
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Beau's Lines in Mucocutaneous Lymph Node Syndrome

Archives of Pediatrics & Adolescent Medicine, 1981
To the Editor .—In an excellent review of mucocutaneous lymph node syndrome (MLNS) by Yanagihara and Todd (Journal1980;134:603-614) and more recently in a case report by Glanzer et at, 1 transverse grooves or furrows are described, which appeared one to two months after the illness.
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AN UNCOMMON CLINICAL SIGN IN MUCOCUTANEOUS LYMPH NODE SYNDROME

Acta Paediatrica, 1981
. Verghote, M., Rousseau, E., Jacob, J. L. and Lapointe, N. (Division of Immunology, Department of Pediatrics, Department of Ophthalmology, Hopital Ste-Justine, Universite de Montreal, Quebec, Canada). An uncommon clinical sign in mucocutaneous lymph node syndrome. Acta Paediatr Scand 70:591,.–A cotton wool retinal exudate is described in a 4 6/12 year
J. L. Jacob   +3 more
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Mucocutaneous Lymph Node Syndrome and Hydropic Gallbladders

Pediatrics, 1980
The article by Slovis et al (Pediatrics 65:789, 1980) reports four patients with hydrops of the gallbladder and mucocutaneous lymph node syndrome (MCLNS). Two of the patients, however, have evidence of coincident streptococcal infection, and hence, do not fulfill the criteria for MCLNS. Patients 1 and 4 both have elevated antistreptolysin O and patient
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Mucocutaneous Lymph Node Syndrome (Kawasaki Disease) in Adults

JAMA: The Journal of the American Medical Association, 1980
To the Editor.— The case reports presented by E. Dale Everett, MD (242:542, 1979), purports to describe adult cases of mucocutaneous lymph node syndrome (Kawasaki disease). Before this association becomes ingrained in the general medical literature, I would like to urge a note of caution.
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Kawasaki Disease (Mucocutaneous Lymph Node Syndrome)

1984
Since mucocutaneous lymph node syndrome (MCLS) was first described by Kawasaki in 1967 [1], several environmental agents have been reported to be involved in the disease. However, nothing has been widely accepted, and the involvement of genetic factors in the pathogenesis of MCLS is obscure.
Takehiko Sasazuki   +5 more
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Mucocutaneous lymph node syndrome

Oral Surgery, Oral Medicine, Oral Pathology, 1979
Mucocutaneous lymph node syndrome (MLNS) has been accepted in Japan as a newly recognized disease affecting most frequently patients under 5 years of age. It is now apparent that the syndrome, having been defined, is also recognized with increasing frequency in the continental United States and Canada in children of non-Japanese ancestry.
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Mucocutaneous Lymph Node Syndrome (Kawasaki Disease) in Adults

JAMA: The Journal of the American Medical Association, 1979
Mucocutaneous lymph node syndrome has been reported to occur only in children. Three adults aged 16 to 27 years had findings compatible with this illness. Patients with fever, polymorphous skin eruption, congested conjunctiva, reddened palms and soles, red lips and oral mucous membrane, and soft-tissue swelling of the peripheral extremities and who ...
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