نتایج جستجو برای: consanguinity

تعداد نتایج: 1500  

Journal: :Journal of Psychology and Clinical Psychiatry 2020

Journal: :THE PROFESSIONAL MEDICAL JOURNAL 2017

انواری, ناهید, پورجعفری , حمید ,

In  a  cross-sectional  study, the  frequency and types of consanguinity     marriages in Hamadan city were determined in 1996.          In this study the randomly selected couples were interviewed.          245 cases (23.07%)of 1062 were consanguinous. The most frequent...

Journal: :Egyptian Journal of Medical Human Genetics 2013

Background Intellectual Disability (ID) is a heterogeneous disorder, in which at least 600 genes participate. The present study aimed to identify the effect of genetic counseling and consanguinity marriage in Iranian families with sporadic mental disability. Materials and Methods: In th...

Journal: :acta medica iranica 0
zohreh kavehmanesh department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. zahra khalili matinzadeh department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. susan amirsalari department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. mohammad torkaman department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. shahla afsharpayman department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran. morteza javadipour department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran.

leukocyte adhesion deficiency type 1 (lad 1) is an autosomal recessive hereditary disorder resulting from deficiency of cd18, characterized by recurrent bacterial infections. we report two consanguineous patients with leukocyte adhesion deficiency type 1( lad1). these two infant boy patients were referred to us, within a short period of time, with the complaints of recurrent infections at the a...

2010
Baha Zantour Mohamed Habib Sfar Samia Younes Wafa Alaya Mahdi Kamoun Emna Mkaouar Saida Jerbi

A 45-year-old male was referred for diabetes mellitus. Clinical examination found a family history of multiple precocious deaths, strong consanguinity, personal history of seizures during childhood, small testicles, small penis, sparse body hair, long arms and legs, dysmorphic features, mental retardation, dysarthria, tremor, and mild gait ataxia. Investigations found pigmentary retinitis, meta...

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