The diagnostic umbrella of mental retardation
نویسندگان
چکیده
منابع مشابه
Diagnostic classification of the aetiology of mental retardation in children.
Children with mental retardation are often subjected to a routine battery of tests, a practice that has been criticised.' Investigations often include a blood count, a biochemical profile, urinary screening for metabolites including amino acids, and radiography of the skull and wrist for bone age and may be more extensive. Such routine testing of all children with mental retardation is done in ...
متن کاملDiagnostic evaluation of developmental delay/mental retardation: An overview.
Mental retardation (MR) is one of the few clinically important disorders for which the etiopathogenesis is still poorly understood. It is a condition of great concern for public health and society. MR is currently defined as a significant impairment of cognitive and adaptive functions, with onset before age 18 years. It may become evident during infancy or early childhood as developmental delay...
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Introduction: Fragile X syndrome (FXS) is one of the most prevalent genetic causes of developmental disability, representing the most frequent form of inherited severe cognitive deficit. The present study was undertaken to investigate FXS and its prevalence in moderate mentally retarded people in patients. Materials and methods: Nineteen people with moderate mental retardation (MR) who wer...
متن کاملMental Retardation
This small book is the first of a series of occasional papers which are to be published under the auspices of the Institute for Research into Mental Retardation, and its author is the chairman of the Institute's Research Committee. In the preface, it is said to be aimed at an intelligent lay audience and it is suggested that 'it will be read with interest and profit by workers in the field of m...
متن کاملThe genetics of mental retardation.
Genetic abnormalities frequently give rise to a mental retardation phenotype. Recent advances in resolution of comparative genomic hybridization and genomic sequence annotation has identified new syndromes at chromosome 3q29 and 9q34. The finding of a significant number of copy number polymorphisms in the genome in the normal population, means that assigning pathogenicity to deletions and dupli...
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ژورنال
عنوان ژورنال: Academic Medicine
سال: 1966
ISSN: 1040-2446
DOI: 10.1097/00001888-196609000-00008