Literature DB >> 15301825

Evaluation and management of children with holoprosencephaly.

Jin S Hahn1, Lauren L Plawner.   

Abstract

Recent advances in genetics and neuroimaging have greatly contributed to our understanding of the spectrum of midline brain and craniofacial malformations known as holoprosencephaly. Neuroradiologic studies have provided detailed characteristics of four major types of holoprosencephaly: alobar, semilobar, lobar, and middle interhemispheric variant. Clinical studies in children with these types of holoprosencephaly have revealed a wide range of survival and neurologic outcomes. Motor and developmental dysfunctions correlate with the severity of the brain malformation in holoprosencephaly. These findings have implications in the management of medical problems associated with holoprosencephaly and overall prognostication.

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Year:  2004        PMID: 15301825     DOI: 10.1016/j.pediatrneurol.2004.03.006

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  13 in total

1.  The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes.

Authors:  Aimée D C Paulussen; Constance T Schrander-Stumpel; Demis C J Tserpelis; Matteus K M Spee; Alexander P A Stegmann; Grazia M Mancini; Alice S Brooks; Margriet Collée; Anneke Maat-Kievit; Marleen E H Simon; Yolande van Bever; Irene Stolte-Dijkstra; Wilhelmina S Kerstjens-Frederikse; Johanna C Herkert; Anthonie J van Essen; Klaske D Lichtenbelt; Arie van Haeringen; Mei L Kwee; Augusta M A Lachmeijer; Gita M B Tan-Sindhunata; Merel C van Maarle; Yvonne H J M Arens; Eric E J G L Smeets; Christine E de Die-Smulders; John J M Engelen; Hubertus J Smeets; Jos Herbergs
Journal:  Eur J Hum Genet       Date:  2010-06-09       Impact factor: 4.246

2.  Holoprosencephaly-Associated Hyperkinesia.

Authors:  Marisela E Dy; Nathaniel A Chuang; Jennifer Friedman
Journal:  Mov Disord Clin Pract       Date:  2015-05-09

Review 3.  Diffusion tensor imaging and fiber tractography in brain malformations.

Authors:  Andrea Poretti; Avner Meoded; Andrea Rossi; Charles Raybaud; Thierry A G M Huisman
Journal:  Pediatr Radiol       Date:  2013-01-04

4.  New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.

Authors:  Sandra Mercier; Christèle Dubourg; Nicolas Garcelon; Boris Campillo-Gimenez; Isabelle Gicquel; Marion Belleguic; Leslie Ratié; Laurent Pasquier; Philippe Loget; Claude Bendavid; Sylvie Jaillard; Lucie Rochard; Chloé Quélin; Valérie Dupé; Véronique David; Sylvie Odent
Journal:  J Med Genet       Date:  2011-09-22       Impact factor: 6.318

Review 5.  Holoprosencephaly: a guide to diagnosis and clinical management.

Authors:  Manu S Raam; Benjamin D Solomon; Maximilian Muenke
Journal:  Indian Pediatr       Date:  2011-06       Impact factor: 1.411

6.  Multisystem Involvement in a Patient with a PTCH1 Mutation: Clinical and Imaging Findings.

Authors:  Antonio Richieri-Costa; Siulan Vendramini-Pittoli; Nancy Mizue Kokitsu-Nakata; Roseli Maria Zechi-Ceide; Camila Wenceslau Alvarez; Lucilene Arilho Ribeiro-Bicudo
Journal:  J Pediatr Genet       Date:  2016-09-14

7.  A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrum.

Authors:  Daniel E Pineda-Alvarez; Benjamin D Solomon; Erich Roessler; Joan Z Balog; Donald W Hadley; Wadih M Zein; Casey K Hadsall; Brian P Brooks; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2011-10-04       Impact factor: 2.802

8.  Links between abnormal brain structure and cognition in holoprosencephaly.

Authors:  Cynthia P Roesler; Sarah J Paterson; Judy Flax; Jin S Hahn; Caryn Kovar; Elaine E Stashinko; Hongkui Jing; April A Benasich
Journal:  Pediatr Neurol       Date:  2006-12       Impact factor: 3.372

9.  A preterm infant with semilobar holoprosencephaly and hydrocephalus: a case report.

Authors:  Ashish O Gupta; Patrick Leblanc; Krishna C Janumpally; Pattaraporn Tanya
Journal:  Cases J       Date:  2010-01-22

10.  Semilobarholoprosencephaly - A Dreading Congenital Anomaly.

Authors:  Bhushita B Lakhkar; Bhushan N Lakhkar; Bhavana B Lakhkar
Journal:  J Clin Diagn Res       Date:  2017-06-01
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