Literature DB >> 31384970

Prenatal evaluation of the Sakoda complex.

Usha D Nagaraj1,2, Rohitha Moudgal3, Robert J Hopkin3,4, Charu Venkatesan3,5, Beth M Kline-Fath6,3.   

Abstract

Sakoda complex is a rare but distinct combination of birth defects consisting of a basal cephalocele, agenesis of the corpus callosum, and midline cleft lip/palate. It has been reported in association with ophthalmologic abnormalities, cognitive deficits and severe epilepsy. Here we describe both prenatal and postnatal MRI findings of a classic case of Sakoda complex in a child with characteristic findings on fetal MRI; prenatal findings have not been described in the literature. Diagnosis of this entity has important implications for prenatal counseling and perinatal management, as is demonstrated in this case.

Entities:  

Keywords:  Basal encephalocele; Fetus; Magnetic resonance imaging; Neonate; Sakoda complex

Mesh:

Year:  2019        PMID: 31384970     DOI: 10.1007/s00247-019-04491-5

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  8 in total

1.  Two cases further delineating the Sakoda complex.

Authors:  Melissa A Dempsey; Wilfredo Torres-Martinez; Laurence E Walsh
Journal:  Am J Med Genet A       Date:  2007-02-15       Impact factor: 2.802

2.  Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy.

Authors:  Sibel Kantarci; Nicola K Ragge; N Simon Thomas; David O Robinson; Kristin M Noonan; Meaghan K Russell; Dian Donnai; F Lucy Raymond; Christopher A Walsh; Patricia K Donahoe; Barbara R Pober
Journal:  Am J Med Genet A       Date:  2008-07-15       Impact factor: 2.802

Review 3.  The Morning Glory syndrome associated with sphenoethmoidal encephalocele.

Authors:  M Hope-Ross; S S Johnston
Journal:  Ophthalmic Paediatr Genet       Date:  1990-06

Review 4.  New syndrome with the Sakoda complex, bilateral anophthalmia, and cortical dysgenesis.

Authors:  H Ehara; A Kurimasa; K Ohno; K Takeshita
Journal:  Pediatr Neurol       Date:  1998-05       Impact factor: 3.372

5.  Sphenoethmoidal meningoencephalocele associated with agenesis of corpus callosum and median cleft lip and palate. Case report.

Authors:  K Sakoda; S Ishikawa; T Uozumi; K Hirakawa; H Okazaki; Y Harada
Journal:  J Neurosurg       Date:  1979-09       Impact factor: 5.115

6.  The Syndrome of Frontonasal Dysplasia, Callosal Agenesis, Basal Encephalocele, and Eye Anomalies - Phenotypic and Aetiological Considerations.

Authors:  Antonio Richieri-Costa; Maria Leine Guion-Almeida
Journal:  Int J Med Sci       Date:  2004-03-10       Impact factor: 3.738

7.  Congenital basal meningoceles with different outcomes: a case series.

Authors:  Satomi Okano; Ryosuke Tanaka; Akie Okayama; Etsushi Tsuchida; Fumikatsu Nohara; Nao Suzuki; Toshio Okamoto; Ken Nagaya; Satoru Takahashi; Hiroshi Azuma
Journal:  J Med Case Rep       Date:  2017-12-27

8.  ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies.

Authors:  Emma A Webb; Angham AlMutair; Daniel Kelberman; Chiara Bacchelli; Estelle Chanudet; Francesco Lescai; Cynthia L Andoniadou; Abdul Banyan; Al Alsawaid; Muhammad T Alrifai; Mohammed A Alahmesh; M Balwi; Seyedeh N Mousavy-Gharavy; Biljana Lukovic; Derek Burke; Mark J McCabe; Tessa Kasia; Robert Kleta; Elia Stupka; Philip L Beales; Dorothy A Thompson; W Kling Chong; Fowzan S Alkuraya; Juan-Pedro Martinez-Barbera; Jane C Sowden; Mehul T Dattani
Journal:  Brain       Date:  2013-09-10       Impact factor: 13.501

  8 in total
  1 in total

Review 1.  Clinical Applications of Fetal MRI in the Brain.

Authors:  Usha D Nagaraj; Beth M Kline-Fath
Journal:  Diagnostics (Basel)       Date:  2022-03-21
  1 in total

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