Volume-8 ~ Issue-1
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Abstract: Dermatoglyphic features are inherited by polygenic system with individual gene contributing a small additive effect. The present research aims to primarily study the various dermatoglyphic patterns in the patients of the Maturity Onset Diabetes Mellitus (Type II diabetes) and compare these statistically with the dermatoglyphic patterns in individuals not suffering from it. The present study was carried out on 101 (51 male and 50 female) clinically diagnosed patients of maturity onset diabetes mellitus. Healthy controls (n=100, 50 males and 50 females) were studied for comparison. Palmar prints were obtained in all the patients and controls and the dermatoglyphic patterns were analyzed using statistical considerations. Standard fingertip pattern configurations and landmarks were used in the study. Significantly higher frequency of arches and lower frequency of whorls were observed in female diabetics than controls. Dankmeijer's Index was highest in female diabetic group and Furuhata's Index was highest in the male control group. AFRC and TFRC were significantly lower in diabetic females than controls. Findings of the present study after a meticulous analysis of different fingertip dermatoglyphic variables highlights on the possible markers and indicate that there is scope for further study on a larger sample size.
Keywords- Arches, Dermatoglyphics, Maturity Onset Diabetes Mellitus, Palmar print, Ulnar loops, Radial loops, Whorls
[1] Park K., Park's textbook of preventive and social medicine (15th ed. Jabalpur. India: M/S Banaridas Bhanot, 1997).
[2] Robert FM, Young ID. Emery's elements of Medical genetics (10th ed. Edinburgh London: Churchill Livingstone, 1998). [3] Iqbal MA, Sahay BK, Ahuja YR, Finger and palmar ridge counts in diabetes mellitus, Acta Anthropogenetica 2(3), 1978, 35-38.
[4] Sant SM, Vare AM, Fakhruddin S, Dermatoglyphics in diabetes mellitus, J Anat Soc India 3(2), 1983, 127-30.
[5] Verbov JL, Dermatoglyphics in early onset diabetes mellitus, Human Hered. 23(6), 1973, 535-42. [6] Ravindranath R, Thomas IH, Finger ridge count and finger print pattern in maturity onset diabetes mellitus, Ind J Med Sci 49, 1995, 153-156.
[7] Sarthak Sengupta, Jina Borush, Finger dermatoglyphic patterns in diabetes mellitus, J Hum. Ecol7(3), 1996, 203-206.
[8] Vadgaonkar R, Pai M, Prabhu L, Saralaya V, Digito- palmar complex in non-insulin dependent diabetes mellitus, Tuek J Med Sci. 36(6), 2006, 353-35.
[9] Barta L, Regoly-Merei A, Kammerer L, Dermatoglyphic features in diabetes mellitus, Acta Paediatr Acad Sci Hung. 19(1), 1978, 31-4.
[10] Mandasesu S, Richards B, Cadman J, Detection of prediabetics by palmar prints: a computor based study leading to a low cost tool. Available at:http//atlas.ici.echoto/MEDNIF99/papers/Benard/detection of pre.htm
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Abstract: Background: For diagnosis of Lower respiratory tract infections (LRTIs), expectorated sputum is the most commonly received sample in the laboratory. Normal resident bacteria of the oropharynx usually contaminate the sputum sample. The value of sputum microscopy and culture in the diagnosis, management and outcome of LRTIs is a matter of controversy. The following study was conducted to evaluate the correlation of Gram's stain and culture in sputum samples from LRTIs. Materials & Methods: The present study was during a one year period (January to December 2012). A total of 120 sputum samples were processed . All the samples were processed through Gram's stain and culture. The Gram's smear was examined for the presence of polymorphs, epithelial cells and bacterial forms. Sputum samples were evaluated based on Bartlett's grading system. The cultures were incubated at 370C overnight and identified in a Microscan autoSCAN 4 instrument (SIEMENS). Results And Conclusions: Out of 120 sputum samples processed, 78 (65%) were acceptable and 42 (35%) were not meeting the standard criteria of Bartlett. Potential pathogens were obtained from 70 of 78 acceptable samples (89.74%), and from 4 of 42 non-acceptable samples (9.52%). Gram's stain could detect similar morphological forms as that obtained in culture in 62 of the acceptable samples (sensitivity- 79.48%) and 4 of the non acceptable samples (sensitivity -4.76%). The most common organisms isolated in the present study include: Klebsiella pneumoniae- 22.85%, Streptococcus pneumoniae- 11.49% and Staphylococcus aureus- 10%. As authors of the present study, we recommend initial screening of sputum samples for clinically relevant results, and reject the non-acceptable samples, and re-order for fresh and correct specimens. Key Words: Sputum, Gram's stain, Bartlett's criteria, sputum culture.
[1]. Nihan Ziyade, Aysegul Yagci. Improving sputum culture results for diagnosis of lower respiratory tract infections by saline washing. Marmara Medical Journal, 2010; 23(1): 30-36.
[2]. Ravichandran Theerthakarai, Walid El Halees, Medhat Ismail, Roberto A. Solis, M Anees Khan. Non value of Initial Microbiological Studies in the management of non severe Community Acquired Pneumonia. Chest, January 2001; 119(1): 181-184.
[3]. Washington Winn Jr, Stephen Allen, William Janda, Elmer Koneman. Guidelines for collection, transport, processing, analysis and reporting of cultures from specific specimen sources. In: Koneman's colour atlas and textbook of Microbiology, 6th edition. Lippincott, Williams and Wilkins publications, 2006: 68-111.
[4]. Fuselier PA, Garcin LS, Procop GW. Infections of the Lower Respiratory Tract. In: Betty AF, Daniel FS, Alice SW, editors. Bailey and Scott's Diagnostic Microbiology. Mosby, 2002; 884-898..
[5]. Stavros Anevlavis, Niki Petroglon, Athanasios Tzavaras, Efstratios Maltzos, Ioannis Pneumatikos, Marios Froudarakis, Eleftherios Anevlavis, Demosthenes Bouros. A prospective study of the diagnostic utility of sputum Gram stain in pneumonia. Journal of Infection, 2009; 59: 83-89.
[6]. Mariraj J, Surekha Y, Asangi, Krishna S, Suresh B Sonth, Ramesh, Shanmugam. Sputum Gram's stain assessment in relation to sputum culture for Respiratory Tract Infections in a tertiary care hospital. Journal of Clinical and Diagnostic Research, December 2011; 5(8): 1699-1700.
[7]. Daniel M Musher, Roberto Montoya, Anna Wanahita. Diagnostic value of microscopic examination of Gram stained sputum and sputum cultures in patients with Pneumococcal pneumonia. Clinical Infectious Diseases, 2004; 39: 165-169.
[8]. Jean Jacques Lloveras, Mohamed –Issam, Shukr, Claude Pinos, Anissa Lindoulsi, Philippe Grima. Usefulness of sputum Gram's stain and culture for diagnosis of pneumonia in Geriatric institution. Journal of IMAB, 2010; 16(3): 20-22.
[9]. Nawfal Ali Mubarak. The findings of sputum culture of intubated mechanically ventilated patients versus non intubated patients in the Intensive Care Unit. Basrah Journal of Surgery, September 2012; 18: 1-5.
[10]. Aroma Oberoi, Aruna Aggarwal. Bacteriological profile, Serology and Antibiotic Sensitivity Pattern of Micro-organisms from Community Acquired Pneumonia. J K Science, April-June 2006; 8(2): 79-82.
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| Paper Type | : | Research Paper |
| Title | : | Cell Hydrogen Oxidation |
| Country | : | India |
| Authors | : | Thiyagarajan babu, Chidambaram |
| : | 10.9790/0853-0811015 ![]() |
Abstract:Every individual‟s 75 to 100 trillion (1014) living cells fight with the millions of harmful radicals which were unstable molecules lacking one or more electrons and compensate by damaging healthy cells. Human body posses millions of glands all over the body to provide specialized products like proteins, fatty acids, hormones etc., to take care of any irregularity and inconsistency in the human system. Indeed the specialized glands like lachrymal gland, sweat gland, salivary glands etc., secrete only the essential compounds and those compounds reach cells associating with cellular water to protect the respective organs. The water every human being consumed was converted as cellular water (reduced surface tension and increased wetting ability) at standard ambient temperature and pressure and reverse was not possible in the cell system. The objective of this paper was that "No water molecules were externally released from human skin or any part of human cells except through kidney system." For example watery fluid formation inside the mouth involved different chemical reaction and it mixed with "salivary compounds‟ forming "saliva‟ contrary to existing saliva chemistry. The cell Hydrogen oxidation process was unknown due to the fact tears, saliva, nasal fluid and perspiration had the traces of compounds of respective glands and literatures cited they were the products of respective glands misleading the entire scientific community till date "My review is going to clear all the misconception and cell Hydrogen oxidation (redox potential balance) is explained more appropriately in this paper.
Key words: - Radicals, Glands, Molecules, Dehydration, Oxidation, Hyperhidrosis.
[1]. Gleick, PH., Water in Crisis: A Guide to the World's Freshwater Resources. Table 2.1 "Water reserves on the earth."Oxford University Press. 1993; p 13. [2]. Guyton, Arthur C. Textbook of Medical Physiology (5th ed.). Philadelphia: W.B. Saunders. 1976; p. 424. ISBN 0-7216-4393-0. [3]. "MDG Report 2008". Retrieved 2010-07-25.
[4]. Re: What percentage of the human body is composed of water? Jeffrey Utz, M.D., The MadSci Network.
[5]. Drink at least eight glasses of water a day." Really? Is there scientific evidence for "8 × 8"? by Heinz Valdin, Department of Physiology, Dartmouth Medical School, Lebanon, New Hampshire.
[6]. Food and Nutrition Board, National Academy of Sciences. Recommended Dietary Allowances. National Research Council, Reprint and Circular Series, No. 122. 1945; pp. 3–18.
[7]. "Eye, human."Encyclopædia Britannica from Encyclopædia Britannica, 2006; Ultimate Reference Suite DVD 2009.
[8]. Thiyagarajan Babu, , Noble Ganga Tears-Sweat Bomb Theory, (IOSR-JNHS) e-ISSN: 2320–1959.p- ISSN: 2320–1940. 2013; 1 (3) , 52-54.
[9]. Skorucak A. "The Science of Tears." ScienceIQ.com. Accessed September 29, 2006. [10]. Holly FJ, Lemp MA, , Tear physiology and dry eyes, Surv Ophthalmol, 1977; Sep-Oct; 22 (2) : 69-87.
