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  • 1
    ISSN: 1573-2622
    Keywords: African-American race ; glaucoma ; pigmentary glaucoma ; pigment dispersion syndrome ; secondary glaucoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Purpose: To investigate the racial heritage of a group of African-Americans who exhibit the pigment dispersion syndrome (PDS). Subjects and Methods: Ten unrelated African-American PDS patients (age range 13–59) from a primary eye care population in Chicago, Illinois, USA, were interviewed to determine their racial heritage. Since Caucasian and Native American heritage were commonly reported, 101 unaffected African-American control subjects (age range 18–55) were also interviewed to determine the reported frequency of these specific racial heritage characteristics. Results: Some degree of Caucasian heritage was reported by 100% of the PDS subjects and by 46.5% of controls. Native American heritage was reported by 90% of the PDS subjects and by 71.3% of controls. Based on these data, the PDS subjects were significantly more likely to report Caucasian heritage (Fisher's exact test, P=0.001) but they were not significantly more likely to report Native American heritage (P=0.282). In addition, the PDS subjects were significantly more likely to report Caucasian heritage from both parents (P=0.024) and more likely to report a combination of both Caucasian and Native American heritage (P=0.0006) than corresponding controls. In general, the PDS subjects had `light' or `medium' complexions. Conclusion: Results from this analysis are consistent with the hypothesis that non-African heritage, particularly Caucasian, is likely to be prevalent in the background of African-Americans who exhibit PDS. It is suggested that non-African heritage may not only be important for the transference of PDS causing genes, but it may also influence factors such as degree of iris pigmentation and rigidity which could influence iris contour and the subsequent expression of PDS in those who are genetically predisposed. Further investigation is needed to study the factors that influence the expression and severity of PDS among African-Americans, a population which traditionally has been considered to be rarely affected by this condition.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Electron microscopic studies reveal that the red pulp of the rabbit spleen is composed of reticular cells, reticulum and elements of the blood circulating through it. The three types of reticular cells described follow no definite pattern as to types of spaces they line and are not always adjacent to a basement membrane. Similar or dissimilar cells may line a basement membrane on the same or opposing sides. The entire red pulp area is intercommunicating through pores and junctions of the several spaces and in that area in which no basement membrane exists, the cytoplasmic projections of the reticular cells form a meshwork of spaces. Terminal arterioles are seen to end in collapsed type channels with a change from endothelium to Type I reticular cells. These rapidly join dilated areas. The reticular network of the spleen appears as four types: homogeneous, fibrillar, a combination of these, and reticular cells only. Isolated cilia are found in the reticular cell cytoplasm and are shown to be associated with a basal body and a centriole. The investigation supported the hypothesis that the red pulp of the spleen in the adult rabbit is a functionally dynamic area constantly changing its histological structure, both regarding cells and state of the vascular channels.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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