Literature DB >> 3146304

Frontonasal "dysplasia," cerebral anomalies, and polydactyly: report of a new syndrome and discussion from a developmental field perspective.

H V Toriello1, L L Radecki, J Sharda, D Looyenga, R Mann.   

Abstract

We describe a boy with frontonasal "dysplasia"; cerebral anomalies, including agenesis of corpus callosum and probable Dandy-Walker malformation (absent superior vermis, hypoplastic cerebellum and brain stem, and possible posterior fossa cyst in this case); short neck, relatively long trunk with short limbs; cryptorchidism; and polydactyly of hands and feet. We suspect he has a previously undescribed syndrome of presently unknown cause. We also discuss this case from a developmental field perspective, in view of the unusual combination of cerebral and facial defects.

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Year:  1986        PMID: 3146304     DOI: 10.1002/ajmg.1320250613

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  4 in total

1.  Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia.

Authors:  Elif Uz; Yasemin Alanay; Dilek Aktas; Ibrahim Vargel; Safak Gucer; Gokhan Tuncbilek; Ferdinand von Eggeling; Engin Yilmaz; Ozgur Deren; Nicole Posorski; Hilal Ozdag; Thomas Liehr; Sevim Balci; Mehmet Alikasifoglu; Bernd Wollnik; Nurten A Akarsu
Journal:  Am J Hum Genet       Date:  2010-05-06       Impact factor: 11.025

2.  Craniofrontonasal dysplasia.

Authors:  L Kapusta; H G Brunner; B C Hamel
Journal:  Eur J Pediatr       Date:  1992-11       Impact factor: 3.183

3.  Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis.

Authors:  Joshua D Smith; Anne V Hing; Christine M Clarke; Nathan M Johnson; Francisco A Perez; Sarah S Park; Jeremy A Horst; Brig Mecham; Lisa Maves; Deborah A Nickerson; Michael L Cunningham
Journal:  Am J Hum Genet       Date:  2014-08-07       Impact factor: 11.025

4.  A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity.

Authors:  S Cataltepe; E Tuncbilek
Journal:  Eur J Pediatr       Date:  1992-04       Impact factor: 3.183

  4 in total

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