Literature DB >> 26500966

Middle Interhemispheric Variant of Holoprosencephaly - Presenting as Non-Visualized Cavum Septum Pellucidum and An Interhemispheric Cyst in A 19-Weeks Fetus.

Akhila Vasudeva1, Shalini S Nayak2, Rajagopal Kadavigere3, Katta M Girisha4, Jyothi Shetty5.   

Abstract

Middle Interhemispheric variant (MIH) is a rare subtype of holoprosencephaly (HPE), also known as syntelencephaly. We present a case of MIH, which was diagnosed as an interhemispheric cyst on antenatal sonography at 19 weeks, but later diagnosed as MIH variant of holoprosencephaly after a postabortal MRI and perinatal autopsy.

Entities:  

Keywords:  Arachnoid cyst; Interhemispheric fissure; Ventriculomegaly

Year:  2015        PMID： 26500966      PMCID： PMC4606295          DOI： 10.7860/JCDR/2015/14076.6525

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN： 0973-709X


  11 in total

1.  Middle interhemispheric variant of holoprosencephaly: a very mild clinical case.

Authors:  R Biancheri; A Rossi; P Tortori-Donati; S Stringara; S Bonifacino; C Minetti
Journal:  Neurology       Date:  2004-12-14       Impact factor: 9.910

2.  Prenatal diagnosis of a possible new middle interhemispheric variant of holoprosencephaly using sonographic and magnetic resonance imaging.

Authors:  O Picone; R Hirt; B Suarez; A Coulomb; G Tachdjian; R Frydman; M-V Senat
Journal:  Ultrasound Obstet Gynecol       Date:  2006-08       Impact factor: 7.299

3.  Clinical image. Middle interhemispheric variant of holoprosencephaly.

Authors:  Marcela Posada; Mauricio Castillo
Journal:  Pediatr Radiol       Date:  2009-12-08

4.  Segregation analysis in nonsyndromic holoprosencephaly.

Authors:  S Odent; B Le Marec; A Munnich; M Le Merrer; C Bonaïti-Pellié
Journal:  Am J Med Genet       Date:  1998-05-01

5.  Differential diagnosis in fetuses with absent septum pellucidum.

Authors:  G Malinger; D Lev; D Kidron; F Heredia; R Hershkovitz; T Lerman-Sagie
Journal:  Ultrasound Obstet Gynecol       Date:  2005-01       Impact factor: 7.299

6.  Unusual variant of holoprosencephaly in monosomy 13q.

Authors:  Pascale Marcorelles; Philippe Loget; Catherine Fallet-Bianco; Joëlle Roume; Ferechte Encha-Razavi; Anne-Lise Delezoide
Journal:  Pediatr Dev Pathol       Date:  2002 Mar-Apr

7.  Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.

Authors:  L Y Brown; S Odent; V David; M Blayau; C Dubourg; C Apacik; M A Delgado; B D Hall; J F Reynolds; A Sommer; D Wieczorek; S A Brown; M Muenke
Journal:  Hum Mol Genet       Date:  2001-04-01       Impact factor: 6.150

8.  EYA4, deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts with SIX3 both physically and functionally.

Authors:  Yuichi Abe; Akira Oka; Masashi Mizuguchi; Takashi Igarashi; Shumpei Ishikawa; Hiroyuki Aburatani; Shigetoshi Yokoyama; Hiroshi Asahara; Kazuaki Nagao; Masao Yamada; Toshiyuki Miyashita
Journal:  Hum Mutat       Date:  2009-10       Impact factor: 4.878

9.  Prenatal MR findings of the middle interhemispheric variant of holoprosencephaly.

Authors:  Steven B Pulitzer; Erin M Simon; Timothy M Crombleholme; Jeffrey A Golden
Journal:  AJNR Am J Neuroradiol       Date:  2004 Jun-Jul       Impact factor: 3.825

10.  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
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.