Literature DB >> 22965664

Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsis.

Hannah M Tully1, Jennifer C Dempsey, Gisele E Ishak, Margaret P Adam, Cynthia J R Curry, Pedro Sanchez-Lara, Alasdair Hunter, Karen W Gripp, Judith Allanson, Christopher Cunniff, Ian Glass, Kathleen J Millen, Daniel Doherty, William B Dobyns.   

Abstract

Rhombencephalosynapsis (RES) is an uncommon cerebellar malformation characterized by fusion of the hemispheres without an intervening vermis. Frequently described in association with Gómez-López-Hernández syndrome, RES also occurs in conjunction with VACTERL features and with holoprosencephaly (HPE). We sought to determine the full phenotypic spectrum of RES in a large cohort of patients. Information was obtained through database review, patient questionnaire, radiographic, and morphologic assessment, and statistical analysis. We assessed 53 patients. Thirty-three had alopecia, 3 had trigeminal anesthesia, 14 had VACTERL features, and 2 had HPE with aventriculy. Specific craniofacial features were seen throughout the cohort, but were more common in patients with alopecia. We noted substantial overlap between groups. We conclude that although some distinct subgroups can be delineated, the overlapping features seen in our cohort suggest an underlying spectrum of RES-associated malformations rather than a collection of discrete syndromes.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22965664      PMCID: PMC3448816          DOI: 10.1002/ajmg.a.35561

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


  53 in total

1.  ZIC2 mutations are seen in holoprosencephaly and not partial rhombencephalosynapsis.

Authors:  Saurabh Guleria
Journal:  Am J Med Genet A       Date:  2011-10-11       Impact factor: 2.802

2.  Rhombencephalosynapsis with massive hydrocephalus: case report and pathogenetic considerations.

Authors:  Anthony T Yachnis
Journal:  Acta Neuropathol       Date:  2001-11-22       Impact factor: 17.088

3.  Gomez-Lopez-Hernandez syndrome: expansion of the phenotype.

Authors:  D Brocks; M Irons; A Sadeghi-Najad; R McCauley; P Wheeler
Journal:  Am J Med Genet       Date:  2000-10-23

4.  Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity.

Authors:  Gisele E Ishak; Jennifer C Dempsey; Dennis W W Shaw; Hannah Tully; Margaret P Adam; Pedro A Sanchez-Lara; Ian Glass; Tessa C Rue; Kathleen J Millen; William B Dobyns; Dan Doherty
Journal:  Brain       Date:  2012-03-26       Impact factor: 13.501

5.  Aprosencephaly: histopathological features of the rudimentary forebrain and retina.

Authors:  A Kakita; S Hayashi; M Arakawa; H Takahashi
Journal:  Acta Neuropathol       Date:  2001-07       Impact factor: 17.088

Review 6.  Molecular genetic classification of central nervous system malformations.

Authors:  H B Sarnat
Journal:  J Child Neurol       Date:  2000-10       Impact factor: 1.987

7.  Defects of blastogenesis: counseling dilemmas in two families.

Authors:  G de Jong; P A Kirby
Journal:  Am J Med Genet       Date:  2000-03-20

8.  Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtype.

Authors:  A J Lewis; E M Simon; A J Barkovich; N J Clegg; M R Delgado; E Levey; J S Hahn
Journal:  Neurology       Date:  2002-12-24       Impact factor: 9.910

Review 9.  Congenital triangular alopecia: a case report and review.

Authors:  Kathleen B Elmer; Rita M George
Journal:  Cutis       Date:  2002-04

Review 10.  Rhombencephalosynapsis: clinical findings and neuroimaging in 9 children.

Authors:  S P Toelle; C Yalcinkaya; N Kocer; T Deonna; W C G Overweg-Plandsoen; T Bast; R Kalmanchey; P Barsi; J F L Schneider; A Capone Mori; E Boltshauser
Journal:  Neuropediatrics       Date:  2002-08       Impact factor: 1.947

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  7 in total

Review 1.  Rhombencephalosynapsis: Fused cerebellum, confused geneticists.

Authors:  Kimberly A Aldinger; Jennifer C Dempsey; Hannah M Tully; Megan E Grout; Michele G Mehaffey; William B Dobyns; Dan Doherty
Journal:  Am J Med Genet C Semin Med Genet       Date:  2018-12       Impact factor: 3.908

2.  MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis.

Authors:  Christopher C Y Mak; Dan Doherty; Angela E Lin; Nancy Vegas; Megan T Cho; Géraldine Viot; Clémantine Dimartino; James D Weisfeld-Adams; Davor Lessel; Shelagh Joss; Chumei Li; Claudia Gonzaga-Jauregui; Yuri A Zarate; Nadja Ehmke; Denise Horn; Caitlin Troyer; Sarina G Kant; Youngha Lee; Gisele E Ishak; Gordon Leung; Amanda Barone Pritchard; Sandra Yang; Eric G Bend; Francesca Filippini; Chelsea Roadhouse; Nicolas Lebrun; Michele G Mehaffey; Pierre-Marie Martin; Benjamin Apple; Francisca Millan; Oliver Puk; Mariette J V Hoffer; Lindsay B Henderson; Ruth McGowan; Ingrid M Wentzensen; Steven Pei; Farah R Zahir; Mullin Yu; William T Gibson; Ann Seman; Marcie Steeves; Jill R Murrell; Sabine Luettgen; Elizabeth Francisco; Tim M Strom; Louise Amlie-Wolf; Angela M Kaindl; William G Wilson; Sara Halbach; Lina Basel-Salmon; Noa Lev-El; Jonas Denecke; Lisenka E L M Vissers; Kelly Radtke; Jamel Chelly; Elaine Zackai; Jan M Friedman; Michael J Bamshad; Deborah A Nickerson; Russell R Reid; Koenraad Devriendt; Jong-Hee Chae; Elliot Stolerman; Carey McDougall; Zöe Powis; Thierry Bienvenu; Tiong Y Tan; Naama Orenstein; William B Dobyns; Joseph T Shieh; Murim Choi; Darrel Waggoner; Karen W Gripp; Michael J Parker; Joan Stoler; Stanislas Lyonnet; Valérie Cormier-Daire; David Viskochil; Trevor L Hoffman; Jeanne Amiel; Brian H Y Chung; Christopher T Gordon
Journal:  Brain       Date:  2020-01-01       Impact factor: 13.501

Review 3.  Infantile hydrocephalus: a review of epidemiology, classification and causes.

Authors:  Hannah M Tully; William B Dobyns
Journal:  Eur J Med Genet       Date:  2014-06-13       Impact factor: 2.708

4.  Ataxia and developmental delay as the main manifestation of rhombencephalosynapsis.

Authors:  Mohammad Paktinat; Soroor Inaloo; Zahra Serati; Eslam Shorafa
Journal:  Iran J Neurol       Date:  2018-01-05

Review 5.  Midbrain and hindbrain malformations: advances in clinical diagnosis, imaging, and genetics.

Authors:  Dan Doherty; Kathleen J Millen; A James Barkovich
Journal:  Lancet Neurol       Date:  2013-03-18       Impact factor: 44.182

6.  Gomez-López-Hernández syndrome: A case report with clinical and molecular evaluation and literature review.

Authors:  Eduardo Perrone; Vânia D'Almeida; Nara Lygia de Macena Sobreira; Claudia Berlim de Mello; Allan Chiaratti de Oliveira; Stênio Burlin; Maria de Fátima de Faria Soares; Mirlene Cecília Soares Pinho Cernach; Ana Beatriz Alvarez Perez
Journal:  Am J Med Genet A       Date:  2020-04-17       Impact factor: 2.802

7.  Diagnosis of rhomboencephalosynapsis by MRI in a 5-year-old child.

Authors:  Nathalia Tafur Gómez; William Prada Mancilla; Carlos Hernán Roa Mejía; Juan Carlos Aldana Leal
Journal:  Radiol Case Rep       Date:  2020-05-01
  7 in total

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