Literature DB >> 23917590

Neuroimaging findings in children with Keutel syndrome.

Thangamadhan Bosemani1, Ryan J Felling, Emily Wyse, Monica S Pearl, Aylin Tekes, Edward Ahn, Andrea Poretti, Thierry A G M Huisman.   

Abstract

BACKGROUND: Keutel syndrome is a rare autosomal-recessive condition characterized by abnormal cartilage calcification. Neuroimaging findings associated with this condition have been randomly described in the literature.
OBJECTIVE: To systematically evaluate the neuroimaging findings in a series of children with Keutel syndrome to broaden our base of knowledge.
MATERIALS AND METHODS: Four children with confirmed Keutel syndrome were reviewed for the brain, head and neck imaging findings.
RESULTS: Three of the four children, all siblings, showed evidence of moyamoya syndrome. All four siblings had pinna cartilage calcification.
CONCLUSION: We propose that Keutel syndrome be considered and included among the secondary causes of moyamoya syndrome. In children with petrified auricle and neurological symptoms, Keutel syndrome should be considered and brain MRI with MRA is required.

Entities:  

Mesh:

Year:  2013        PMID: 23917590     DOI: 10.1007/s00247-013-2768-0

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


  11 in total

Review 1.  Auricular ossificans (ectopic ossification of the auricle).

Authors:  P Craig Stites; Alan S Boyd; John Zic
Journal:  J Am Acad Dermatol       Date:  2003-07       Impact factor: 11.527

2.  Petrified ears in a patient with Keutel syndrome: temporal bone CT findings.

Authors:  Hemant Parmar; Susan Blaser; Sheila Unger; Shi-Joon Yoo; Blake Papsin
Journal:  Pediatr Radiol       Date:  2005-11-18

Review 3.  A novel MGP mutation in a consanguineous family: review of the clinical and molecular characteristics of Keutel syndrome.

Authors:  David J Hur; Gerald V Raymond; Stephen G Kahler; Douglas L Riegert-Johnson; Bernard A Cohen; Simeon A Boyadjiev
Journal:  Am J Med Genet A       Date:  2005-05-15       Impact factor: 2.802

Review 4.  Keutel syndrome: further characterization and review.

Authors:  A S Teebi; D M Lambert; G M Kaye; S Al-Fifi; T L Tewfik; E M Azouz
Journal:  Am J Med Genet       Date:  1998-06-30

5.  Tracheobronchial stenosis in Keutel syndrome.

Authors:  M Meier; L P Weng; E Alexandrakis; J Rüschoff; G Goeckenjan
Journal:  Eur Respir J       Date:  2001-03       Impact factor: 16.671

6.  Spontaneous calcification of arteries and cartilage in mice lacking matrix GLA protein.

Authors:  G Luo; P Ducy; M D McKee; G J Pinero; E Loyer; R R Behringer; G Karsenty
Journal:  Nature       Date:  1997-03-06       Impact factor: 49.962

7.  Moyamoya disease and syndrome.

Authors:  H J Hoffman
Journal:  Clin Neurol Neurosurg       Date:  1997-10       Impact factor: 1.876

Review 8.  Moyamoya disease and moyamoya syndrome.

Authors:  R Michael Scott; Edward R Smith
Journal:  N Engl J Med       Date:  2009-03-19       Impact factor: 91.245

9.  Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome.

Authors:  P B Munroe; R O Olgunturk; J P Fryns; L Van Maldergem; F Ziereisen; B Yuksel; R M Gardiner; E Chung
Journal:  Nat Genet       Date:  1999-01       Impact factor: 38.330

10.  Mechanisms of arterial remodeling: lessons from genetic diseases.

Authors:  Bernard J van Varik; Roger J M W Rennenberg; Chris P Reutelingsperger; Abraham A Kroon; Peter W de Leeuw; Leon J Schurgers
Journal:  Front Genet       Date:  2012-12-13       Impact factor: 4.599

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