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Clinical aspect of sjorgen`s syndrome

by M. Arief Setiawan, Yoga I. Kasjmir, Harry Isbagio ([Publisher not identified] , 2002)

 Abstrak

Sjorgen's syndrome (SS) is a chronic rheumatic autoimmune disease characterized by specific symptoms of sicca keratocon junctivitis (SKC) and xerostomia (called Sicca complex) due to decreased secretion of the lacrimal and salivary glands, with or without enlargement of the parotid gland.1'3
SS is said to be the second most common autoimmune rheumatic disease after Rheumatoid Arthritis (RA), and is even more common than SLE. However, SS is a disease that is very hard to diagnose.3 The average time between the onset and diagnosis is approximately 8-9 years. As with other autoimmune diseases, it is most commonly found among women, with a ratio of approximately 9:1.3A
Treatment of SS will always involve many experts, such as neurologists, ophthalmologists, pulmonologists, dermatologists, ENT specialists, gynecologists, and of course, rheumatologists.4*5

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 Metadata

No. Panggil : AMIN-XXXIV-2-AprJun2002-65
Entri utama-Nama orang :
Entri tambahan-Nama orang :
Penerbitan : [Place of publication not identified]: [Publisher not identified], 2002
Sumber Pengatalogan :
ISSN :
Majalah/Jurnal : Acta Medica Indonesiana
Volume : Vol. XXXIV (2) April-June 2002: 65-70
Tipe Konten :
Tipe Media :
Tipe Carrier :
Akses Elektronik :
Institusi Pemilik : Universitas Indonesia
Lokasi :
  • Ketersediaan
  • Ulasan
No. Panggil No. Barkod Ketersediaan
AMIN-XXXIV-2-AprJun2002-65 03-20-987093351 TERSEDIA
Ulasan:
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