Literature DB >> 8544809

State-specific rates of mental retardation--United States, 1993.

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Abstract

Mental retardation (MR) is the most common developmental disability and ranks first among chronic conditions causing major activity limitations among persons in the United States (1). National and state-specific surveillance to measure the prevalence of MR can assist in targeting areas of need and allocating resources. State-specific prevalences for MR can be determined by using data about persons who receive specialized services for MR through entitlement programs. To estimate state-specific prevalences of MR in 1993, data were analyzed from the U.S. Department of Education (DOE) for children with MR who were enrolled in special education programs and from the Social Security Administration (SSA) for adults with MR. This report summarizes the findings, which suggest substantial state-specific variation in the prevalence of MR in the United States.

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Year:  1996        PMID: 8544809

Source DB:  PubMed          Journal:  MMWR Morb Mortal Wkly Rep        ISSN: 0149-2195            Impact factor:   17.586


  7 in total

1.  A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation.

Authors:  Joseph J Higgins; Joanna Pucilowska; Roni Q Lombardi; John P Rooney
Journal:  Neurology       Date:  2004-11-23       Impact factor: 9.910

2.  A mental retardation-linked nonsense mutation in cereblon is rescued by proteasome inhibition.

Authors:  Guoqiang Xu; Xiaogang Jiang; Samie R Jaffrey
Journal:  J Biol Chem       Date:  2013-08-27       Impact factor: 5.157

3.  Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features.

Authors:  Qing Ouyang; Tojo Nakayama; Ozan Baytas; Shawn M Davidson; Chendong Yang; Michael Schmidt; Sofia B Lizarraga; Sasmita Mishra; Malak Ei-Quessny; Saima Niaz; Mirrat Gul Butt; Syed Imran Murtaza; Afzal Javed; Haroon Rashid Chaudhry; Dylan J Vaughan; R Sean Hill; Jennifer N Partlow; Seung-Yun Yoo; Anh-Thu N Lam; Ramzi Nasir; Muna Al-Saffar; A James Barkovich; Matthew Schwede; Shailender Nagpal; Anna Rajab; Ralph J DeBerardinis; David E Housman; Ganeshwaran H Mochida; Eric M Morrow
Journal:  Proc Natl Acad Sci U S A       Date:  2016-09-06       Impact factor: 11.205

Review 4.  Exome sequencing and the genetics of intellectual disability.

Authors:  S Topper; C Ober; Soma Das
Journal:  Clin Genet       Date:  2011-06-15       Impact factor: 4.438

5.  Modifying a social problem-solving program with the input of individuals with intellectual disabilities and their staff.

Authors:  Sarah H Ailey; Tanya R Friese; Arthur M Nezu
Journal:  Res Nurs Health       Date:  2012-07-02       Impact factor: 2.228

6.  Dysregulation of large-conductance Ca2+-activated K+ channel expression in nonsyndromal mental retardation due to a cereblon p.R419X mutation.

Authors:  Joseph J Higgins; Jin Hao; Barry E Kosofsky; Anjali M Rajadhyaksha
Journal:  Neurogenetics       Date:  2008-04-15       Impact factor: 2.660

7.  A newborn with ambiguous genitalia and a complex X;Y rearrangement.

Authors:  Mohammadreza Dehghani; Elena Rossi; Annalisa Vetro; Gianni Russo; Zahra Hashemian; Orsetta Zuffardi
Journal:  Iran J Reprod Med       Date:  2014-05
  7 in total

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