STUDY OF MYOPIA MORPHOMETRIC INDICES IN CHILDREN WITH UNDIFFERENTIATED CONNECTIVE TISSUE DYSPLASIA
نویسندگان
چکیده
منابع مشابه
inductive effect of palatal connective tissue on alveolar mocosa after subepithelial connective tissue graft clinical & histologic study
چکیده ندارد.
15 صفحه اولUndifferentiated connective tissue diseases (UCTD).
The term undifferentiated connective tissue diseases is used to define conditions characterized by the presence of signs and symptoms suggestive of a systemic autoimmune disease that do not satisfy the classificative criteria for defined connective tissue diseases (CTD) such as systemic lupus erythematosus (SLE), Sjögren's syndrome (SS), rheumatoid arthritis (RA) and others. A small percentage ...
متن کاملUndifferentiated connective tissue diseases in 2004.
The existence of patients with signs and symptoms suggestive of a systemic autoimmune disease but not fulfilling the classification criteria for defined diseases is a common experience in clinical practice. The first description of these diseases dates back to 1980, when LeRoy proposed the term "Undifferentiated Connective Tissue Syndromes" (UCTS) to define the early phases of connective tissue...
متن کاملprevalence of atopic dermatitis in children with type 1 diabetes mellitus in southeastern of iran (kerman province): a case-control study
چکیده ندارد.
15 صفحه اول[Calcic tenosynovitis in a patient with undifferentiated connective tissue disease].
1699-258X/$ see front matter © 2010 Elsevier España, S.L. All rights reserved. We present the case of a 50 year old woman who was diagnosed with undifferentiated connective tissue disease (UCTD), based on severe Raynaud’s phenomenon with ischemic ulcers, extensive calcinosis, sclerodactilia, polyarthritis, glomerulonephritis, polyserositis, chronic hypertransaminasemia and had undergone the bil...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Bulletin of Problems Biology and Medicine
سال: 2018
ISSN: 2077-4214,2523-4110
DOI: 10.29254/2077-4214-2018-2-144-189-193