Literature DB >> 1642232

Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

P J Willems1, L Vits, P Raeymaekers, J Beuten, P Coucke, J J Holden, C Van Broeckhoven, S T Warren, M Sagi, D Robinson.   

Abstract

X-linked hydrocephalus (HSAS) is the most frequent genetic form of hydrocephalus. Clinical symptoms of HSAS include hydrocephalus, mental retardation, clasped thumbs, and spastic paraparesis. Recently we have assigned the HSAS gene to Xq28 by linkage analysis. In the present study we used a panel of 18 Xq27-q28 marker loci to further localize the HSAS gene in 13 HSAS families of different ethnic origins. Among the Xq27-q28 marker loci used, DXS52, DXS15, and F8C gave the highest combined lod scores, of 14.64, 6.53 and 6.33, respectively, at recombination fractions of .04, 0, and .05, respectively. Multipoint linkage analysis localizes the HSAS gene in the telomeric part of the Xq28 region, with a maximal lod score of 20.91 at 0.5 cM distal to DXS52. Several recombinations between the HSAS gene and the Xq28 markers DXS455, DXS304, DXS305, and DXS52 confirm that the HSAS locus is distal to DXS52. One crossover between HSAS and F8C suggests that HSAS gene to be proximal to F8C. Therefore, data from multipoint linkage analysis and the localization of key crossovers indicate that the HSAS gene is most likely located between DXS52 and F8C. This high-resolution genetic mapping places the HSAS locus within a region of less than 2 Mb in length, which is now amenable to positional cloning.

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Year:  1992        PMID: 1642232      PMCID: PMC1682663     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  31 in total

1.  MspI RFLP in the L1 CAM gene in Xq28.

Authors:  P J Willems; L Vits; K De Boulle
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

2.  Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomere.

Authors:  L M Mulligan; H J Grover; V S Blanchette; A R Giles; D P Lillicrap; A Phillips; J J Holden; B N White
Journal:  Am J Med Genet       Date:  1987-03

3.  MASA syndrome: further clinical delineation and chromosomal localisation.

Authors:  R M Winter; K E Davies; M V Bell; S M Huson; M N Patterson
Journal:  Hum Genet       Date:  1989-07       Impact factor: 4.132

4.  Report of the committee on linkage and gene order.

Authors:  B Keats; J Ott; M Conneally
Journal:  Cytogenet Cell Genet       Date:  1989

5.  Autosomal recessive nonsyndromal hydrocephalus.

Authors:  A S Teebi; K K Naguib
Journal:  Am J Med Genet       Date:  1988-10

6.  Heterogeneity in familial hydrocephalus.

Authors:  P J Willems
Journal:  Am J Med Genet       Date:  1988-10

7.  A contiguous, 3-Mb physical map of Xq28 extending from the colorblindness locus to DXS15.

Authors:  S Kenwrick; J Gitschier
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

8.  The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

Authors:  H Veenema; N J Carpenter; E Bakker; M H Hofker; A M Ward; P L Pearson
Journal:  J Med Genet       Date:  1987-07       Impact factor: 6.318

9.  X-linked hydrocephalus.

Authors:  P J Willems; O F Brouwer; I Dijkstra; J Wilmink
Journal:  Am J Med Genet       Date:  1987-08

10.  Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

Authors:  S Kenwrick; V Ionasescu; G Ionasescu; C Searby; A King; M Dubowitz; K E Davies
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

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  10 in total

1.  Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

Authors:  L Strain; A F Wright; D T Bonthron
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

Review 2.  X linked hydrocephalus and MASA syndrome.

Authors:  S Kenwrick; M Jouet; D Donnai
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

3.  Five novel mutations in the L1CAM gene in families with X linked hydrocephalus.

Authors:  S M Gu; U Orth; A Veske; H Enders; K Klunder; M Schlosser; W Engel; E Schwinger; A Gal
Journal:  J Med Genet       Date:  1996-02       Impact factor: 6.318

4.  A new mutation of the L1CAM gene in an X-linked hydrocephalus family.

Authors:  S Izumoto; M Yamasaki; N Arita; S Hiraga; T Ohnishi; K Fujitani; S Sakoda; T Hayakawa
Journal:  Childs Nerv Syst       Date:  1996-12       Impact factor: 1.475

5.  A gene for dominant nonspecific X-linked mental retardation is located in Xq28.

Authors:  V des Portes; P Billuart; A Carrié; L Bachner; T Bienvenu; M C Vinet; C Beldjord; G Ponsot; A Kahn; J Boué; J Chelly
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

6.  Discordant segregation of Xq28 markers and a mutation in the L1 gene in a family with X linked hydrocephalus.

Authors:  M Jouet; L Strain; D Bonthron; S Kenwrick
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

7.  Refining the genetic location of the gene for X linked hydrocephalus within Xq28.

Authors:  M Jouet; E Feldman; J Yates; D Donnai; J Paterson; D Siggers; S Kenwrick
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

8.  Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3.

Authors:  L Strain; C M Gosden; D J Brock; D T Bonthron
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

9.  Detection of L1 CAM mutation in a male child with mental retardation.

Authors:  M Swarna; M Sujatha; P Usha Rani; P P Reddy
Journal:  Indian J Clin Biochem       Date:  2004-07

10.  Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia.

Authors:  Y Saillour; G Zanni; V Des Portes; D Heron; L Guibaud; M T Iba-Zizen; J L Pedespan; K Poirier; L Castelnau; C Julien; C Franconnet; D Bonthron; M E Porteous; J Chelly; T Bienvenu
Journal:  J Med Genet       Date:  2007-07-06       Impact factor: 6.318

  10 in total

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