نتایج جستجو برای: genetic abnormalities

تعداد نتایج: 704179  

Apert syndrome is a genetic defect which was first described by Eugene Apert in 1906. itchr('39')s incidence is approximately one in 50000 births. This syndrome is many abnormalities in your body and Central Nervous System. rehabilitation can increase children and their parentchr('39')s quality of life.We report a case of Apert syndrome and his occupational therapy program.

Journal: :journal of research in medical sciences 0
leila etemad department of pharmacodynamics and toxicology, school of pharmacy, mashhad university of medical sciences, mashhad, iran mohammad moshiri department of pharmacodynamics and toxicology, school of pharmacy, mashhad university of medical sciences, mashhad, iran seyed a moallem department of pharmacodynamics and toxicology, school of pharmacy, mashhad university of medical sciences and pharmaceutical sciences research center and medical toxicology research center, mashhad university of medical sciences, mashhad, iran

normal 0 false false false en-us x-none ar-sa approximately 1% of all pregnancies are in woman with epilepsy. although, the majority of children born to women with epilepsy are normal, they are at increased risk for malformations. notably, the teratogenicity of antiepileptic drugs is a well-defined subject. the incidence of major malformations in offspring of mothers with epilepsy who were trea...

رزم پا, ابراهیم, سلطان سنجری, مصطفی, عظیمی, سیروس, قاسم‌پور, عادل, نظری, حسین, یوسفی, مریم,

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Journal: :Asian Journal of Animal and Veterinary Advances 2011

Aflatoonian A Ghasemi N, Jahaninejad T Zare S

Background: Recurrent pregnancy loss (RPL) is a multifactorial problem associated with genetic abnormalities reflected by inherited disorders. The aim of the present study was to investigate the contribution of heterochromatin polymorphism in couples with recurrent miscarriages compared with couples without miscarriages. Materials and Methods: Over a 3 year period, we made a study of the diagno...

Hamid Gourabi Iman Salahshourifar, Mohammad Ali Sadighi Gilani, Najmeh sadat Masoudi

Background The present study offers our contribution on the topic by a retrospective analysis of the prevalence of chromosomal abnormalities in a population of Iranian infertile men attending assisted reproduction programs. MaterialsAndMethods Cytogenetic analysis was performed according to standard methods on cultured cells obtained from the patient peripheral blood. In all, 874 files belongin...

Journal: :iranian rehabilitation journal 0
masoud gharib pediatric neurorehabilitation research center . university of social welfare and rehabilitation science,tehran,iran nazila akbar fahimi phd student of occupational therapy, occupational therapy department, university of social welfare and rehabilitation science,tehran,iran

apert syndrome is a genetic defect which was first described by eugene apert in 1906. it's incidence is approximately one in 50000 births. this syndrome is many abnormalities in your body and central nervous system. rehabilitation can increase children and their parent's quality of life.we report a case of apert syndrome and his occupational therapy program.

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