نتایج جستجو برای: consanguinity marriage genetic counseling

تعداد نتایج: 659401  

Journal: :مجله پزشکی مولکولی 0
pooneh nikuei molecular medicine research center, hormozgan university of medical sciences, bandar abbas, iran mehrdad mohtarami fertility and infertility research center, hormozgan university of medical sciences, bandar abbas, iran mohsen azad student research committee, hormozgan university of medical sciences, bandar abbas, iran fatemeh mohseni molecular medicine research center, hormozgan university of medical sciences, bandar abbas, iran fouzieh hajizadeh medical genetic counseling center, social welfare organization, bandar abbas, iran

introduction: mental retardation, is one of the most common causes for referral to genetic counseling centers, and is one of the greatest challenges in health care services in the world. down syndrome is the most common chromosomal abnormalities in humans. methods: this study performed in medical genetic counseling center of welfare organization in south of iran with high consanguineous marriag...

Journal: :International journal of epidemiology 2009
A H Bittles

During the early years of Christianity there were major social and legal differences in attitude towards consanguineous marriage in the Eastern and Western Roman empires, reflecting pre-existing divisions between the Classical Greek and Roman worlds. In Athens and Sparta first-cousin, uncle–niece and half-sib marriages were permissible, with half-sib marriage, and even full-sib marriage continu...

Journal: :Human reproduction 2001
B Baccetti S Capitani G Collodel G Di Cairano L Gambera E Moretti P Piomboni

BACKGROUND The existence of a genetic component to human infertility has been suggested, although neither the specific abnormalities involved, nor their genetic mechanism of transmission, are currently defined. We have examined, by transmission electron microscopy (TEM), ejaculate from 1600 males with fertility problems. Among the subjects studied, we focused on a group of patients whose family...

2018
Maryam NAZEMIPOUR Abdol-Mohammad KAJBAFZADEH Kazem MOHAMMAD Abbas RAHIMI FOROUSHANI Asal HOJJAT Maryam SEYEDTABIB Ali NAZEMIPOUR Mahmood MAHMOUDI

Background The aim of this study was comparison characteristics of family and demographics of children with antenatal hydronephrosis, in 2nd and 3rd trimester of pregnancy, in order to the need for postnatal management. Methods This cross-sectional study described some information from family of children with antenatal hydronephrosis, at the Pediatric Urology Research Center of Children's Hos...

Journal: :Croatian medical journal 2007
Emna Kerkeni Kamel Monastiri Besma Saket Mohamed Neji Guediche Hassen Ben Cheikh

AIM To assess the association among social status, prevalence of consanguineous marriages, and the effects of consanguinity on reproductive behavior and mortality in Tunisia. METHODS The study included data on a total of 1741 live-births born from November 1989 to October 1990 in the maternity ward of the University-Hospital Fattouma Bourguiba of Monastir, Tunisia. After delivery, women fille...

Journal: :Applied sciences 2022

The aim of this study was to determine the prevalence dental anomalies and whethera significant association exists between consanguinity marriage among Arabic orthodontic patients in Israel. Pretreatment panoramic radiographs 513 (38% males 62% females) were examined detect related number, size, shape, eruption. A chi-square test carried out associations anomalies, gender, marriage. results ind...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: :American journal of medical genetics. Part A 2014
Sheela Nampoothiri Dhanya Yesodharan Gazel Sainulabdin Dhanyalakshmi Narayanan Laxmi Padmanabhan Katta Mohan Girisha Sara S Cathey Anne De Paepe Fransiska Malfait Delfien Syx Raoul C Hennekam Luisa Bonafe Sheila Unger Andrea Superti-Furga

We report on a series of 514 consecutive diagnoses of skeletal dysplasia made over an 8-year period at a tertiary hospital in Kerala, India. The most common diagnostic groups were dysostosis multiplex group (n = 73) followed by FGFR3 (n = 49) and osteogenesis imperfecta and decreased bone density group (n = 41). Molecular confirmation was obtained in 109 cases. Clinical and radiographic evaluat...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید