Literature DB >> 14608648

Oculo-facio-cardio-dental syndrome: skewed X chromosome inactivation in mother and daughter suggest X-linked dominant Inheritance.

Peter Hedera1, Jerome L Gorski.   

Abstract

Oculo-facio-cardio-dental syndrome (OFCD) is an uncommon multiple congenital anomaly syndrome that is characterized by congenital cataracts, multiple minor facial dysmorphic features, congenital heart defects, and dental anomalies including canine radiculomegaly and oligodontia. Although most cases of OFCD are sporadic, since all reported OFCD individuals have been female, it has been suggested that OFCD is an X-linked dominant trait. Here we report two affected female patients with OFCD, a mother and daughter, who both had congenital cataracts, microphthalmia, characteristic dental anomalies, and typical facial dysmorphisms. These features were diagnostic for OFCD; thus, these cases represent the second documented instance of mother-to-daughter OFCD transmission. In addition to the clinical features typically seen in OFCD individuals, the affected daughter exhibited several additional congenital anomalies including intestinal malrotation and hypoplastic thumbs. Thus, these cases further define and expand the OFCD clinical phenotype. These two individuals also displayed a skewed pattern of X chromosome inactivation. Together, these data strongly support the hypothesis that OFCD is inherited as an X-linked dominant condition. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 14608648     DOI: 10.1002/ajmg.a.20444

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  23 in total

1.  Expression of Normal or Mutated X-Linked BCOR Transcripts in OFCD iPSCs.

Authors:  I El Ayachi; X-Y Zou; X Yan; Y Lou; G T-J Huang
Journal:  J Dent Res       Date:  2019-11-27       Impact factor: 6.116

Review 2.  Oculofaciocardiodental syndrome: a rare case and review of the literature.

Authors:  Amirparviz Davoody; I-Ping Chen; Ravindra Nanda; Flavio Uribe; Ernst J Reichenberger
Journal:  Cleft Palate Craniofac J       Date:  2011-07-08

3.  Evidence of Germline Mosaicism for a Novel BCOR Mutation in Two Indian Sisters with Oculo-Facio-Cardio-Dental Syndrome.

Authors:  Sumita Danda; Vanessa A van Rahden; Deepa John; Padma Paul; Renu Raju; Santosh Koshy; Kerstin Kutsche
Journal:  Mol Syndromol       Date:  2014-08-01

4.  Molecular characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl.

Authors:  Yong-hui Jiang; Ping Fang; Adekunle M Adesina; Patricia Furman; Jennifer J Johnston; Leslie G Biesecker; Chester W Brown
Journal:  Am J Med Genet A       Date:  2009-06       Impact factor: 2.802

5.  Bcl6a function is required during optic cup formation to prevent p53-dependent apoptosis and colobomata.

Authors:  Jiwoon Lee; Bum-Kyu Lee; Jeffrey M Gross
Journal:  Hum Mol Genet       Date:  2013-05-12       Impact factor: 6.150

6.  Oculofaciocardiodental syndrome: novel BCOR mutations and expression in dental cells.

Authors:  Thunyaporn Surapornsawasd; Takuya Ogawa; Michiko Tsuji; Keiji Moriyama
Journal:  J Hum Genet       Date:  2014-04-03       Impact factor: 3.172

7.  Characterization of Bcor expression in mouse development.

Authors:  Joseph A Wamstad; Vivian J Bardwell
Journal:  Gene Expr Patterns       Date:  2007-01-31       Impact factor: 1.224

8.  BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects.

Authors:  Emma Hilton; Jennifer Johnston; Sandra Whalen; Nobuhiko Okamoto; Yoshikazu Hatsukawa; Juntaro Nishio; Hiroshi Kohara; Yoshiko Hirano; Seiji Mizuno; Chiharu Torii; Kenjiro Kosaki; Sylvie Manouvrier; Odile Boute; Rahat Perveen; Caroline Law; Anthony Moore; David Fitzpatrick; Johannes Lemke; Florence Fellmann; François-Guillaume Debray; Florence Dastot-Le-Moal; Marion Gerard; Josiane Martin; Pierre Bitoun; Michel Goossens; Alain Verloes; Albert Schinzel; Deborah Bartholdi; Tanya Bardakjian; Beverly Hay; Kim Jenny; Kathreen Johnston; Michael Lyons; John W Belmont; Leslie G Biesecker; Irina Giurgea; Graeme Black
Journal:  Eur J Hum Genet       Date:  2009-04-15       Impact factor: 4.246

Review 9.  BCOR gene alterations in hematologic diseases.

Authors:  Paolo Sportoletti; Daniele Sorcini; Brunangelo Falini
Journal:  Blood       Date:  2021-12-16       Impact factor: 22.113

10.  BCOR regulates mesenchymal stem cell function by epigenetic mechanisms.

Authors:  Zhipeng Fan; Takayoshi Yamaza; Janice S Lee; Jinhua Yu; Songlin Wang; Guoping Fan; Songtao Shi; Cun-Yu Wang
Journal:  Nat Cell Biol       Date:  2009-07-05       Impact factor: 28.824

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