Literature DB >> 1799424

X-linked mental retardation with Marfanoid habitus: a changing phenotype with age?

J P Fryns1, H Van Den Berghe.   

Abstract

In this report, we present two further examples of X-linked mental retardation with Marfanoid habitus. Follow-up data on these two patients reveal that the clinical diagnosis of this syndrome is extremely difficult, if not impossible before puberty, as the Marfanoid habitus only becomes strikingly evident during adolescence.

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Year:  1991        PMID: 1799424

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  3 in total

1.  The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene.

Authors:  Charles E Schwartz; Patrick S Tarpey; Herbert A Lubs; Alain Verloes; Melanie M May; Hiba Risheg; Michael J Friez; P Andrew Futreal; Sarah Edkins; Jon Teague; Sylvain Briault; Cindy Skinner; Astrid Bauer-Carlin; Richard J Simensen; Sumy M Joseph; Julie R Jones; Josef Gecz; Michael R Stratton; F Lucy Raymond; Roger E Stevenson
Journal:  J Med Genet       Date:  2007-03-16       Impact factor: 6.318

Review 2.  Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus).

Authors:  Griet Van Buggenhout; Jean-Pierre Fryns
Journal:  Orphanet J Rare Dis       Date:  2006-07-10       Impact factor: 4.123

3.  Lujan-Fryns Syndrome (LFS): A Unique Combination of Hypernasality, Marfanoid Body Habitus, and Neuropsychiatric Issues, Presenting as Acute-Onset Dysphagia.

Authors:  Abidullah Khan; Mohammad Humayun; Iqbal Haider; Maimoona Ayub
Journal:  Clin Med Insights Case Rep       Date:  2016-12-04
  3 in total

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