Literature DB >> 3398009

Clinical features and reproductive patterns in fragile X female heterozygotes.

D Z Loesch1, D A Hay.   

Abstract

Clinical findings are presented on 113 fragile X female heterozygotes from 44 families, based on physical examination, behavioural assessment, and reproductive history. In 85% of a subsample of 92 adult females non-verbal IQ score derived from the Block Design test was 85 or less. Verbal ability deficits were much less common. Typical facial characteristics, irregular teeth, and hypermobility of finger joints occurred in approximately 40% of adult females, but facial abnormalities were less common in children. Some physical anomalies and the level of intellectual impairment were, in adult carriers, associated with the presence of fragile X sites. The commoner physical anomalies or typical facial characteristics and intellectual abilities differed significantly between the known female heterozygotes and their 40 presumed normal relatives. Frequency of miscarriages was increased in fragile X females; in spite of this, a moderate increase in the number of children has been encountered in female carriers with borderline intellectual impairment. This important problem has genetical implications and needs further investigation. The importance is emphasised of a more detailed clinical examination of the females at risk in fragile X families.

Entities:  

Mesh:

Year:  1988        PMID: 3398009      PMCID: PMC1050510          DOI: 10.1136/jmg.25.6.407

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  10 in total

1.  CONGENITAL ANOMALIES IN THE NEWBORN INFANT, INCLUDING MINOR VARIATIONS. A STUDY OF 4,412 BABIES BY SURFACE EXAMINATION FOR ANOMALIES AND BUCCAL SMEAR FOR SEX CHROMATIN.

Authors:  P M MARDEN; D W SMITH; M J MCDONALD
Journal:  J Pediatr       Date:  1964-03       Impact factor: 4.406

2.  Phenotypic variation in male-transmitted fragile X: genetic inferences.

Authors:  D Z Loesch; D A Hay; G R Sutherland; J Halliday; C Judge; G C Webb
Journal:  Am J Med Genet       Date:  1987-06

3.  The female and the fragile X. A study of 144 obligate female carriers.

Authors:  J P Fryns
Journal:  Am J Med Genet       Date:  1986 Jan-Feb

4.  The marker (X) syndrome: a cytogenetic and genetic analysis.

Authors:  S L Sherman; N E Morton; P A Jacobs; G Turner
Journal:  Ann Hum Genet       Date:  1984-01       Impact factor: 1.670

Review 5.  Marker (X)-linked mental retardation.

Authors:  G Turner; P Jacobs
Journal:  Adv Hum Genet       Date:  1983

6.  Mutation and selection in the marker (X) syndrome. A hypothesis.

Authors:  F Vogel
Journal:  Ann Hum Genet       Date:  1984-10       Impact factor: 1.670

7.  Detection of the fragile X chromosome and other fragile sites.

Authors:  G C Webb
Journal:  Clin Genet       Date:  1985-05       Impact factor: 4.438

8.  Individual variation and specific cognitive deficits in the fra(X) syndrome.

Authors:  T M Theobald; D A Hay; C Judge
Journal:  Am J Med Genet       Date:  1987-09

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.  Cognitive profiles and the spectrum of clinical manifestations in heterozygous fra (X) females.

Authors:  M B Kemper; R J Hagerman; R S Ahmad; R Mariner
Journal:  Am J Med Genet       Date:  1986 Jan-Feb
  10 in total
  15 in total

1.  Fixed and random effects in the variation of the finger ridge count: a study of fragile-X families.

Authors:  D Z Loesch; R M Huggins
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  "Are We Done Yet?" Question-Asking in Boys With Fragile X Syndrome and Idiopathic Autism Spectrum Disorder.

Authors:  Laura Friedman; Emily Lorang; Elizabeth Hilvert; Audra Sterling
Journal:  J Speech Lang Hear Res       Date:  2020-05-18       Impact factor: 2.297

Review 3.  Fragile X-associated disorders: a clinical overview.

Authors:  Anne Gallagher; Brian Hallahan
Journal:  J Neurol       Date:  2011-07-12       Impact factor: 4.849

4.  Reproductive fitness in familial schizophrenia.

Authors:  A S Bassett; A Bury; K A Hodgkinson; W G Honer
Journal:  Schizophr Res       Date:  1996-09-18       Impact factor: 4.939

5.  Between-generation differences in ascertainment and penetrance: relevance to genetic hypotheses in fragile X.

Authors:  D Z Loesch; L J Sheffield; D A Hay
Journal:  Hum Genet       Date:  1993-06       Impact factor: 4.132

6.  Autism spectrum phenotype in males and females with fragile X full mutation and premutation.

Authors:  Sally Clifford; Cheryl Dissanayake; Quang M Bui; Richard Huggins; Annette K Taylor; Danuta Z Loesch
Journal:  J Autism Dev Disord       Date:  2007-04

7.  Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardation.

Authors:  D Wöhrle; P Steinbach
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

8.  Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.

Authors:  A McConkie-Rosell; A M Lachiewicz; G A Spiridigliozzi; J Tarleton; S Schoenwald; M C Phelan; P Goonewardena; X Ding; W T Brown
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

9.  Couples at risk for spinocerebellar ataxia type 2: the Cuban prenatal diagnosis experience.

Authors:  Tania Cruz-Mariño; Luis Velázquez-Pérez; Yanetza González-Zaldivar; Raúl Aguilera-Rodríguez; Miguel Velázquez-Santos; Yaimé Vázquez-Mojena; Annelié Estupiñán-Rodríguez; Rubén Reynaldo-Armiñán; Luis Enrique Almaguer-Mederos; José Miguel Laffita-Mesa; Victor Tamayo-Chiang; Milena Paneque
Journal:  J Community Genet       Date:  2013-05-15

10.  Are ovarian response and pregnancy rates similar in selected FMR1 premutated and mutated patients undergoing preimplantation genetic testing?

Authors:  Noemie Ranisavljevic; Mathilde Hess; Christel Castelli; Marjolene Willems; Alice Ferrieres-Hoa; Anne Girardet; Tal Anahory
Journal:  J Assist Reprod Genet       Date:  2020-06-02       Impact factor: 3.412

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