Literature DB >> 7081157

Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin.

N J Carpenter, L G Leichtman, B Say.   

Abstract

Fragile X-linked mental retardation is a recently described entity that includes a chromosomal fragile site at Xq28 and macro-orchidism. We studied 50 institutionalized males and 15 noninstitutionalized males and found six (9.2%) with this disorder. Their clinical findings include enlarged testicular volumes, low IQs (30 to 40), perseverative speech patterns, and characteristic facial features, including prominent supraorbital ridges, prognathism, and large ears. We recommend cytogenetic studies for both males and females with mental retardation of unknown origin in order to establish early diagnoses and to extend proper genetic counseling to the affected families.

Entities:  

Mesh:

Year:  1982        PMID: 7081157

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  12 in total

1.  The fragile X syndrome in a large family. I. Cytogenetic and clinical investigations.

Authors:  H Veenema; J P Geraedts; G C Beverstock; P L Pearson
Journal:  J Med Genet       Date:  1987-01       Impact factor: 6.318

2.  Screening for fra(X)(q) in a population of mentally retarded males.

Authors:  U Froster-Iskenius; G Felsch; C Schirren; E Schwinger
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q).

Authors:  J Paul; U Froster-Iskenius; W Moje; E Schwinger
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Clinico-neurological investigations in the fra(X) form of mental retardation.

Authors:  P Vieregge; U Froster-Iskenius
Journal:  J Neurol       Date:  1989-02       Impact factor: 4.849

Review 5.  The fragile X syndrome: the patients and their chromosomes.

Authors:  M A De Arce; A Kearns
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318

6.  Additional evidence for fragile X activity in heterozygous carriers.

Authors:  I A Uchida; V C Freeman; H Jamro; M W Partington; H C Soltan
Journal:  Am J Hum Genet       Date:  1983-09       Impact factor: 11.025

7.  Metacarpophalangeal pattern profile analysis in fragile X syndrome.

Authors:  M G Butler; M Fletcher; D D Gale; F J Meaney; D R McLeod; J Fagan; N J Carpenter
Journal:  Am J Med Genet       Date:  1988-12

8.  Frequency of the fragile X syndrome in Japanese mentally retarded males.

Authors:  T Arinami; I Kondo; S Nakajima
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

9.  Further segregation analysis of the fragile X syndrome with special reference to transmitting males.

Authors:  S L Sherman; P A Jacobs; N E Morton; U Froster-Iskenius; P N Howard-Peebles; K B Nielsen; M W Partington; G R Sutherland; G Turner; M Watson
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X.

Authors:  K B Nielsen; N Tommerup; H Poulsen; P Jacobsen; B Beck; M Mikkelsen
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.