Literature DB >> 1605219

Clasped-thumb mental retardation (MASA) syndrome: confirmation of linkage to Xq28.

V R Macias1, D W Day, T E King, G N Wilson.   

Abstract

We describe a 5-generation Hispanic family with 13 males and 1 female affected with MASA syndrome. The proposita, a 17-year-old female, and her affected male relatives shared many of the cognate manifestations--mental retardation (14/14), aphasia or delayed speech (13/13), shuffling gait (8/13), adduction of thumbs (14/14)--as well as scoliosis (2/13) and increased deep tendon reflexes in the lower extremities (10/13). Southern analysis with the polymorphic DNA probes DXS14 (Xp11), DXS72 (Xq21), and F8C (Xq28) confirmed linkage to the Xq28 region with a maximum lod score of 3.01 for this family.

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Year:  1992        PMID: 1605219     DOI: 10.1002/ajmg.1320430162

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  7 in total

Review 1.  X linked hydrocephalus and MASA syndrome.

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

2.  A deletion of five nucleotides in the L1CAM gene in a Japanese family with X-linked hydrocephalus.

Authors:  T Takechi; J Tohyama; T Kurashige; K Maruta; K Uyemura; T Ohi; S Matsukura; N Sakuragawa
Journal:  Hum Genet       Date:  1996-03       Impact factor: 4.132

3.  CRASH syndrome: mutations in L1CAM correlate with severity of the disease.

Authors:  M Yamasaki; P Thompson; V Lemmon
Journal:  Neuropediatrics       Date:  1997-06       Impact factor: 1.947

4.  Role of the cytoplasmic domain of the L1 cell adhesion molecule in brain development.

Authors:  Yukiko Nakamura; Suni Lee; Candace L Haddox; Eli J Weaver; Vance P Lemmon
Journal:  J Comp Neurol       Date:  2010-04-01       Impact factor: 3.215

Review 5.  Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counselling.

Authors:  C Schrander-Stumpel; J P Fryns
Journal:  Eur J Pediatr       Date:  1998-05       Impact factor: 3.183

6.  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

7.  Genotype-phenotype correlation in L1 associated diseases.

Authors:  E Fransen; G Van Camp; R D'Hooge; L Vits; P J Willems
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

  7 in total

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