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1.
Odontology ; 98(1): 89-96, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20155514

ABSTRACT

Rabson-Mendenhall syndrome is a rare, autosomal recessive disorder characterized by insulin resistance syndrome, growth retardation, coarse and senile-looking faces, mental precocity, early dentition, and pineal hyperplasia. Mutations of the insulin receptor gene affecting insulin action appear to be the basic mechanism underlying this syndrome. We report on Rabson-Mendenhall syndrome in two siblings and briefly review the literature.


Subject(s)
Donohue Syndrome/complications , Malocclusion/complications , Tooth Diseases/complications , Adolescent , Child, Preschool , Donohue Syndrome/pathology , Female , Humans , Malocclusion/diagnosis , Malocclusion/therapy , Siblings , Tooth Diseases/diagnosis , Tooth Diseases/therapy
2.
Indian J Dent Res ; 20(3): 298-303, 2009.
Article in English | MEDLINE | ID: mdl-19884712

ABSTRACT

OBJECTIVES: This study was undertaken to detect the gene polymorphism of detoxification enzymes and estimate the antioxidant enzyme status in patients with oral cancer, oral leukoplakia and oral submucous fibrosis (OSF). MATERIALS AND METHODS: The GSTM1 and GSTT1 gene polymorphism was evaluated using polymerase chain reaction; the antioxidant enzyme was estimated using biochemical methods. Statistical analyses were performed using student t-test and odds-ratio to estimate relative risk (RR). RESULTS: The RR at 95% confidence interval (CI) for GSTM1 and GSTT1 was statistically significant for all groups. The mean values of glutathione were significantly raised in all groups. The mean values of ceruloplasmin and malonaldehyde was statistically significant among cancer and OSF patients but was insignificant in smokers and cases with leukoplakia. CONCLUSION: Several genes perform the same function which implies the need to test for several genetic polymorphisms to identify individuals at high risk. The level of antioxidant enzymes correlate with the degree of oxidative damage. The need for further studies is emphasised.


Subject(s)
Glutathione Transferase/genetics , Leukoplakia/genetics , Mouth Neoplasms/genetics , Oral Submucous Fibrosis/genetics , Precancerous Conditions/genetics , Adult , Aged , Antioxidants/metabolism , Case-Control Studies , Ceruloplasmin/metabolism , Glutathione/metabolism , Humans , Malondialdehyde/metabolism , Matched-Pair Analysis , Middle Aged , Odds Ratio , Polymorphism, Genetic , Reference Values , Statistics, Nonparametric , Young Adult
3.
Int J Cardiol ; 87(1): 9-28; discussion 29-30, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12468050

ABSTRACT

OBJECTIVES: To review mechanisms of circadian variations in heart rate variability (HRV) and blood pressure variability (BPV) and mortality and morbidity due to cardiovascular diseases (CVD). METHODS: Results from 7-day/24-h HRV and BPV are interpreted by gender and age-specified reference values in the context of a Medline search. RESULTS: Abnormal HRV and BPV measured around the clock for 7 days provides information on the risk of subsequent morbid events in subjects without obvious heart disease and without abnormality outside the conventional (in the sense of chronobiologically unquantified) physiological range. Meditation, beta-blockers, ACE inhibitors, n-3 fatty acids and estrogens may have a beneficial influence on HRV, but there is no definitive outcome-validated therapy. Low HRV has been associated with a risk of arrhythmias and arrhythmic death, unstable angina, myocardial infarction, progression of heart failure and atherosclerosis. BPV may be characterized by treatable circadian-hyper-amplitude-tension (CHAT), which can be transient '24-h CHAT' or '7-day-CHAT', MESOR-hypertension and/or an unusually-timed (odd) circadian acrophase (ecphasia), all associated with an increased risk of stroke, stroke death, myocardial infarction, and kidney disease. CONCLUSIONS: Precise insight into the patho-physiology in time of HRV and BPV is needed with development of a consensus on best measures of HRV for clinical purposes and to determine when a 7-day record interpreted chronobiologically suffices and when it does not, for detection within as well as outside the conventional normal range, for diagnostic clinical practice and to direct therapy of risk greater than that associated with hypertension, smoking or any other risk factor.


Subject(s)
Blood Pressure/physiology , Cardiovascular Diseases/physiopathology , Circadian Rhythm/physiology , Heart Rate/physiology , Cardiovascular Diseases/mortality , Death, Sudden, Cardiac/prevention & control , Disease Progression , Humans , Risk Factors
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