Literature DB >> 11170096

Cervical stenosis secondary to rhizomelic chondrodysplasia punctata.

A J Khanna1, N E Braverman, D Valle, P D Sponseller.   

Abstract

Rhizomelic chondrodysplasia punctata (RCDP) is a rare peroxisomal disorder leading to multiple developmental malformations, including skeletal deformity. Specifically, involvement of the vertebral bodies has been described. Presented here is a case of a two-year-old female child with RCDP leading to advanced cervical stenosis as detected on magnetic resonance imaging (MRI) studies of the cervical spine. The practicing clinician should be aware of the possibility of cervical stenosis secondary to RCDP and its impact on the management of the patient with this rare disease process. Copyright Wiley-Liss. Inc.

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Year:  2001        PMID: 11170096     DOI: 10.1002/1096-8628(20010215)99:1<63::aid-ajmg1117>3.0.co;2-9

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  10 in total

Review 1.  Natural history and management of cervical spine disease in chondrodysplasia punctata and coumarin embryopathy.

Authors:  Timothy W Vogel; Arnold H Menezes
Journal:  Childs Nerv Syst       Date:  2012-01-25       Impact factor: 1.475

Review 2.  Plasmalogens and fatty alcohols in rhizomelic chondrodysplasia punctata and Sjögren-Larsson syndrome.

Authors:  Ana R Malheiro; Tiago Ferreira da Silva; Pedro Brites
Journal:  J Inherit Metab Dis       Date:  2014-11-29       Impact factor: 4.982

3.  Specific entities affecting the craniocervical region: syndromes affecting the craniocervical junction.

Authors:  Arnold H Menezes; Timothy W Vogel
Journal:  Childs Nerv Syst       Date:  2008-03-28       Impact factor: 1.475

Review 4.  From peroxisomal disorders to common neurodegenerative diseases - the role of ether phospholipids in the nervous system.

Authors:  Fabian Dorninger; Sonja Forss-Petter; Johannes Berger
Journal:  FEBS Lett       Date:  2017-09-07       Impact factor: 4.124

5.  Clinical and radiological pictures of two newborn babies with manifestations of chondrodysplasia punctata and review of available literature.

Authors:  Elżbieta Jurkiewicz; Beata Marcinska; Joanna Bothur-Nowacka; Anna Dobrzanska
Journal:  Pol J Radiol       Date:  2013-04

6.  A case of rhizomelic chondrodysplasia punctata in newborn.

Authors:  Nalan Karabayır; Gonca Keskindemirci; Erdal Adal; Orhan Korkmaz
Journal:  Case Rep Med       Date:  2014-03-09

Review 7.  Peroxisomes in brain development and function.

Authors:  Johannes Berger; Fabian Dorninger; Sonja Forss-Petter; Markus Kunze
Journal:  Biochim Biophys Acta       Date:  2015-12-11

8.  Common skeletal features in rare diseases: New links between ciliopathies and FGF-related syndromes.

Authors:  Basil Z Yannakoudakis; Karen J Liu
Journal:  Rare Dis       Date:  2013-11-11

9.  Rare Case of Rhizomelic Chondrodysplasia Punctata.

Authors:  Yashwant Mahale; Vikram V Kadu; Amit Chaudhari
Journal:  J Orthop Case Rep       Date:  2015 Jul-Sep

10.  Peroxisome biogenesis disorders.

Authors:  Catherine Argyriou; Maria Daniela D'Agostino; Nancy Braverman
Journal:  Transl Sci Rare Dis       Date:  2016-11-07
  10 in total

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