نتایج جستجو برای: mild mental retardation

تعداد نتایج: 383041  

Journal: :Journal of medical genetics 2003
J Kraus G Lederer C Keri H Seidel I Rost A Wirtz C Fauth M R Speicher

Subtelomeric rearrangements have recently gained considerable interest through publications indicating that they may be a major cause for unexplained mental retardation and/or multiple congenital anomalies. 2 As the subtelomeric regions have the highest gene density in the genome, subtelomeric aneusomies are in general thought to have a significant effect on the phenotype. Prenatal onset of gro...

Journal: :American family physician 2006
Christopher D Prater Robert G Zylstra

Persons with mental retardation are living longer and integrating into their communities. Primary medical care of persons with mental retardation should involve continuity of care, maintenance of comprehensive treatment documentation, routine periodic health screening, and an understanding of the unique medical and behavioral disorders common to this population. Office visits can be successful ...

Journal: :Journal of moral education 2002
Ben Spiecker Jan Steutel

Is sex between people with "mental retardation" [1] morally permissible and, if at all, under what conditions? This paper tries to answer this question, but only with regard to sex between biologically mature individuals with mild or moderate mental retardation. First, the concepts of "sexual activity" and mental retardation" are analysed briefly, which is challenging given the widely divergent...

Journal: :Science 1967

Journal: :Journal of medical genetics 1997
R E Stevenson B Häne J F Arena M May L Lawrence H A Lubs C E Schwartz

A syndrome with distinctive facies, poor muscle tone, absent deep tendon reflexes, tapered fingers, excessive fingerprint arches, genu valgum and mild-moderate mental retardation has occurred in four males in two generations of a white family of European ancestry. The facies are characterised by square configuration, tented upper lip, and thickening of the helices, upper eyelids, and alae nasi....

2016

Deletion of 18p syndrome is characterized by dysmorphic features, growth deficiencies, and mental retardation with a poor verbal performance. Until now, few families have been described with limited clinical description. We report transmission of deletion 18p from a mother to his son. The proband is 8 years old and has short stature, dysmorphic features, polymorphous dyslalia and moderate menta...

Journal: :Orphanet Journal of Rare Diseases 2006
Griet Van Buggenhout Jean-Pierre Fryns

The Lujan-Fryns syndrome or X-linked mental retardation with marfanoid habitus syndrome is a syndromal X-linked form of mental retardation, affecting predominantly males. The prevalence is not known for the general population. The syndrome is associated with mild to moderate mental retardation, distinct facial dysmorphism (long narrow face, maxillary hypoplasia, small mandible and prominent for...

Journal: :دانشور پزشکی 0
دکتر ناصر اصل امین آبادی naser asl aminabadi دکتر عدیله شیرمحمدی adileh shirmohammadi

background & objective : there are over 3 million mental retarded all over the world. so that promotion of oral and dental health of these patients is one of the major challenges in every society. this study was conducted to determine the periodontal treatment needs for these patients in tabriz institutes.   materials & methods : three hundred and eighty six mental retarded patients between 4 t...

Journal: :nursing and midwifery studies 0
zahra aliakbarzadeh-arani department of operating room, faculty of paramedical, qom university of medical sciences, qom, ir iran; department of operating room, faculty of paramedical, qom university of medical sciences, qom, ir iran. tel: +98-9137295893, fax: +98-2517703738

Journal: :journal of basic research in medical sciences 0
asrin karimi reza beiranvand ali delpisheh kourosh sayehmiri asadollah ehsanzadeh

introduction: congenital hypothyroidism is the most common cause of mental retardation in the world. the presence of hypothyroidism in fetal is lead to abnormalities in major organs, including nervous system and central skeleton. aim of this study was to investigate epidemiologic situation of neonatal hypothyroidism in ilam province between 2005 -2011. materials and methods: this was a cross-se...

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