منابع مشابه
Rheumatic Heart Disease in Identical Twins.
Paul (1931) found that the spread of the disease through families suggested that the disease was due to an infection, in which the possible ioles of environment and of an inherited disposition were undetermined. Roberts and Thomson (1934) considered that the most reasonable explanation of the family incidence of the disease was that it is due to genetically determined differences in susceptibil...
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Background/Objective: To clarify the state of different immunologic factors in patients with acute rheumatic fever (ARF) and rheumatic heart disease (RHD) compared to healthy individuals.Patients and Methods: Patients with ARF (#21), patients with RHD six months after the onset of ARF (#19), and healthy children from the same age group with normal physical examination and no history of pharyngi...
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Genetically proven identical twin sisters with Alzheimer's disease are reported. Both sisters at the age of fifty years developed a dementing illness. Their mother and maternal grandmother developed at the same age a similar illness. It is suggested that in some cases of familial Alzheimer's disease the condition is inherited by a single mutant gene.
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Background Tay-Sachs disease is an autosomal-recessive lysosomal storage metabolic disorder. The typical symptoms of the disease include ataxia, muscle weakness, and mental disorders. The severity of the clinical symptom relies on the enzymatic activity of residual Hexosaminidase-A. Case Presentation</...
متن کاملCongenital Cardiac Disease in Identical Twins.
The studv of rare diseases and rare abnormalities is of more valuie in throwing light upon pathological or physiological processes than in furnishing guidance for futuire enc-xunter with the same condition. This principle applies to the study of diseases in the individual, but it applies even more in the case of homogeneous twins, for here the solutions of embryological problems may become appa...
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1940
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.15.83.177