Literature DB >> 6711604

A new X-linked multiple congenital anomalies/mental retardation syndrome.

M Golabi, M Ito, B D Hall.   

Abstract

We report on 2 boys, the sons of sisters, and their mother's brother who have a new, X-linked multiple congenital anomalies/mental retardation (MCA/MR) syndrome. The propositus was a 16-month-old caucasian male with 1) mental retardation, 2) congenital microcephaly, 3) postnatal growth deficiency, 4) ridged metopic suture with narrow bifrontal diameter, 5) upslanted palpebral fissures with persistent epicanthal folds, strabismus, and lacrimal duct obstruction, 6) narrow palate, 7) macrodontia, 8) anteverted ears, 9) atrial septal defect, 10) dry brittle scalp hair and 11) cutis marmorata. His chromosomes were normal. His cousin and uncle were similarly affected. This distinctive MCA/MR syndrome is added to the list of X-linked malformation syndromes known at the present time.

Entities:  

Mesh:

Year:  1984        PMID: 6711604     DOI: 10.1002/ajmg.1320170130

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


  6 in total

Review 1.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

2.  Transient QT interval prolongation in an infant with Simpson-Golabi-Behmel syndrome.

Authors:  Emily Gertsch; Salman Kirmani; Michael J Ackerman; Dusica Babovic-Vuksanovic
Journal:  Am J Med Genet A       Date:  2010-09       Impact factor: 2.802

3.  X linked mental retardation: a family with a separate syndrome?

Authors:  E M Thompson; A Gordon; M Baraitser
Journal:  J Med Genet       Date:  1989-06       Impact factor: 6.318

Review 4.  Molecular insights into the WW domain of the Golabi-Ito-Hall syndrome protein PQBP1.

Authors:  Marius Sudol; Caleb B McDonald; Amjad Farooq
Journal:  FEBS Lett       Date:  2012-03-28       Impact factor: 4.124

5.  Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 gene.

Authors:  H Lubs; F E Abidi; R Echeverri; L Holloway; A Meindl; R E Stevenson; C E Schwartz
Journal:  J Med Genet       Date:  2006-06       Impact factor: 6.318

6.  Familial Sneddon's syndrome.

Authors:  A Lossos; T Ben-Hur; Z Ben-Nariah; C Enk; M Gomori; D Soffer
Journal:  J Neurol       Date:  1995-02       Impact factor: 4.849

  6 in total

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