X-Linked Mental Retardation 3
Read Online
Share

X-Linked Mental Retardation 3 Proceedings of the Third International Workshop on Fragile X and X Linked Mental Retardation Held in Troina, Italy Se by John M. Opitz

  • 920 Want to read
  • ·
  • 19 Currently reading

Published by Wiley-Liss .
Written in English

Subjects:

  • Handicapped,
  • Neurology & clinical neurophysiology,
  • Unassigned Title,
  • Congresses,
  • Fragile X syndrome,
  • Mental Retardation,
  • X-linked mental retardation,
  • familial & genetic,
  • Health/Fitness

Book details:

The Physical Object
FormatHardcover
Number of Pages728
ID Numbers
Open LibraryOL10327762M
ISBN 100471504238
ISBN 109780471504238

Download X-Linked Mental Retardation 3

PDF EPUB FB2 MOBI RTF

This is a comprehensive and up-to-date survey of mental retardation caused by genes on the X chromosome. Clinical and laboratory data on syndromes are presented in a concise and consistent manner. Each syndrome is defined and information is provided on somatic features, growth and development, neurological signs, cognitive performance, imaging and other . X-Linked Mental Retardation Roger E. Stevenson, Charles E. Schwartz, Richard J. Schroer This is a comprehensive and up-to-date survey of mental retardation caused by genes on the X chromosome. Clinical and laboratory data on syndromes are presented in a concise and consistent manner. Summary: "This is a comprehensive, up-to-date and authoritative survey of mental retardation caused by genes on the X chromosome. Clinical and laboratory data on syndromes are presented in a concise and consistent manner. X-linked intellectual disability (previously known as X-linked mental retardation) refers to forms of intellectual disability which are specifically associated with X-linked recessive inheritance.. As with most X-linked disorders, males are more heavily affected than females. Females with one affected X chromosome and one normal X chromosome tend to have milder symptoms.

X-linked mental retardation Definition. X-linked mental retardation (XLMR) broadly refers to a group of inherited disorders characterized by varying degrees of mental retardation, caused by mutations in various genes present on the X chromosome. Mental retardation is defined as the failure to develop cognitive abilities and achieve a level of intelligence and adaptive behavior . ₹ 24, ₹ 19, Book Test. Mental retardation X-linked syndromic Raymond type (ZDHHC9) Test Cost. Raymond et al. X linked mental retardation: a clinical guide. J Med Genet. Mar; 43(3): – Plenge et al. Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders. Am J Hum Genet ; – Vissers et al. Genetic studies in intellectual disability and related disorders. Localization of two X‐linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp‐p and a putative MRX gene on Xp‐p Shirly Bar‐David Israela Lerer.

C R O G Mental retardation 3, X-linked; Clinical features Help List of clinical features of the condition/phenotype displayed from sources such as the Human Phenotype Ontology (HPO) and OMIM. For more information about the disease, please go to the disease information page. mental retardation, X-linked, syndromic, ZDHHC9-related mental retardation, X-linked, with creatine transport deficiency mental retardation, X-linked, with gynaecomastia and obesity. Valerie A. Arboleda, Eric Vilain, in Endocrinology: Adult and Pediatric (Seventh Edition), Alpha-Thalassemia/Mental Retardation, X-Linked (Also Known as X-Linked Helicase 2) Alpha-thalassemia/mental retardation X-linked (ATRX) is a helicase—an enzyme that catalyzes the unwinding of double-stranded nucleic acids—and is a member of a family of proteins involved . Intellectual disability (ID), also known as general learning disability and mental retardation (MR), is a generalized neurodevelopmental disorder characterized by significantly impaired intellectual and adaptive is defined by an IQ un in addition to deficits in two or more adaptive behaviors that affect everyday, general living.. Once focused almost entirely on .