Literature DB >> 21093738

Dandy-Walker malformation: a rare association with hypoparathyroidism.

Dilek Coban1, Mustafa Ali Akin, Selim Kurtoglu, Suat Oktem, Ali Yikilmaz.   

Abstract

Dandy-Walker malformation is characterized by cystic dilatation of the fourth ventricle and an enlarged posterior cranial fossa with upward displacement of the tentorium, lateral sinuses, and torcular, with agenesis or hypoplasia of the cerebellar vermis. Dandy-Walker malformation occurs in approximately the 4th week of gestation and is associated with various abnormalities involving the cardiac, skeletal, genitourinary, and gastrointestinal systems. The parathyroid gland also forms in the 3rd and 4th gestational weeks. Reported here is the case of a male infant with Dandy-Walker malformation with ventricular and atrial septal defect, unilateral renal agenesis, and hypoparathyroidism. To our knowledge, this rare association with neural crest events during the development of Dandy-Walker malformation has not been reported previously. Crown
Copyright © 2010. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21093738     DOI: 10.1016/j.pediatrneurol.2010.06.006

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


  2 in total

1.  Bipolar Disorder in a Young Girl with Dandy-Walker Syndrome.

Authors:  Mahin Eslami Shahre Babaki; Fariborz Estilaee
Journal:  Iran J Psychiatry       Date:  2015-06

2.  Blake's pouch cyst and Werdnig-Hoffmann disease: Report of a new association and review of the literature.

Authors:  Sherien A Shohoud; Waleed A Azab; Tarek M Alsheikh; Rania M Hegazy
Journal:  Surg Neurol Int       Date:  2014-08-21
  2 in total

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