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1.
Int J Pharm Pharm Sci ; 2020 Feb; 12(2): 38-42
Article | IMSEAR | ID: sea-206040

ABSTRACT

Objective: The study focuses on assessing the incidence of menstrual irregularity among young women and the factors for a disturbance with the rationale to assess the use of analgesic drugs during Premenstrual Syndrome (PMS). Methods: A cross-sectional study was used. A total of 2500 randomly selected young female between the age of 11 and 30 y completed the study questionnaire to assess lifestyle pattern, variations in menstrual pattern, perceived stress, and to capture information about their menstrual cycle and related problems. In addition, the questionnaire assessed the use of analgesics for PMS. Results: 2481 participants completed the questionnaire. The mean age of participants’ menarche was 12.85±1.432 y. The prevalence of menstrual irregularities was 25.0 % (n=621) and about 8.5% (n=211) of respondents had severe pain that was not relieved by the use of analgesics. On the other hand, 50.9 % (n=1262) reported severe pain that was relieved by analgesics. A total of 1279 (51.6 %) of participants in this study used Over The Counter (OTC) analgesics to relieve PMS. Conclusion: Dysmenorrhea is the most common complaint among young females in Saudi Arabia. Low Body Mass Index (BMI), sedentary lifestyle, stress and early age of menarche are the most important factors associated with menstrual irregularities. Proper education programs and awareness among young girls about their menstrual health, and the provision of guidance in choosing effective analgesics and treatment options for dysmenorrhea are highly recommended.

2.
Egyptian Journal of Medical Human Genetics [The]. 2011; 12 (1): 79-90
in English | IMEMR | ID: emr-126699

ABSTRACT

In 40-60% of congenital malformations, the cause is unknown. Genetic factors account for approximately 15%; environmental factors produce approximately 10%; a combination of genetic and environmental influences produces 20-25%. The study aims to document prevalence and patterns of congenital malformations detected at birth in Assiut University hospital and clarify underlying chromosomal abnormalities of such malformations. Also possible predisposing factors will be studied. Newborns with apparent congenital anomalies were selected from 5000 newborn infants delivered consecutively at the department of Obstetrics and Gynecology within 7 months. Full maternal history, family history, perinatal history, pedigree construction as well as clinical examinations and investigations including karyotype were done. Congenital anomalies were found in 103 cases with a prevalence of 2.06% with male to female ratio of 1.7:1. Skeletal system anomalies had the highest frequency [37.9%], followed in descending order by chromosomal abnormalities [27.2%], circulatory system anomalies [22.3%], central nervous system [CNS] anomalies [19.4%], genital organs anomalies [16.5%], gastrointestinal tract [GIT] anomalies [14.6%], eye and ear anomalies [8.7%], and lastly urinary system and others anomalies in 3.9% each. Breech presentation, perinatal asphyxia, incubator admission and the need for resuscitation were significantly associated with the presence of congenital anomalies. Higher prevalence of congenital anomalies was observed in neonates of grand multiparous women, diabetic mothers delivery by CS, cases with oligohydramnios and with positive consanguinity. Chromosomal abnormalities were found in 28 cases [27.18% of malformed cases] [5.6/1000]. Numerical abnormalities were found in 22 cases [21.35%] [4.4/1000], Down syndrome in 16 cases, Edward syndrome in two cases, Patau syndrome in one case and Turner syndrome [monosomy] in three cases. Structural abnormalities were present in six cases [5.83%] [1.2/1000], Down syndrome in two cases, Turner syndrome in two cases, balanced translocation [[12;13][q15;q34]] with dysmorphic features and undescended testis in one case and deletion 9[q11;q31] with disorder of sex development in one case. To conclude karyotype should not be done routinely for all malformed cases as many of them are due to genetic syndromes. So, it is more useful to consult expert dysmorphologists for proper syndrome identification and for the decision to use more recent molecular techniques for diagnosis


Subject(s)
Humans , Male , Female , Infant, Newborn , Chromosome Aberrations , Cytogenetic Analysis/methods , Hospitals, University , Cross-Sectional Studies , Karyotyping
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