Literature DB >> 12612818

Brachytelephalangy with sparing of the fifth distal phalanx: a feature highly suggestive of Keutel syndrome.

Stephen F Miller1.   

Abstract

Keutel syndrome (KS) is a rare, autosomal recessive condition characterized by diffuse cartilaginous calcification, nasal hypoplasia, brachytelephalangy, and peripheral pulmonary stenosis. A review of the literature produced only 15 reported patients, of whom plain radiographs of the hand or a detailed report are available for review in ten. A distinctive pattern of broadening and shortening of the first through fourth distal phalanges, with sparing of the fifth distal phalanx, is seen in seven of these patients. Two additional patients with Keutel syndrome and this identical finding are presented. I suggest that this pattern of brachytelephalangy is sensitive and highly suggestive of the diagnosis of Keutel syndrome.

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Year:  2002        PMID: 12612818     DOI: 10.1007/s00247-002-0846-9

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


  10 in total

Review 1.  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

2.  Keutel syndrome: a report of four cases.

Authors:  H E Khosroshahi; O Uluoğlu; R Olguntürk; C Başaklar
Journal:  Eur J Pediatr       Date:  1989-12       Impact factor: 3.183

3.  Keutel syndrome: clinical report and literature review.

Authors:  E J Cormode; M Dawson; R B Lowry
Journal:  Am J Med Genet       Date:  1986-06

4.  Unusual calcium deposition in cartilage associated with short stature and peculiar facial features: a case report.

Authors:  B Say; S Balci; T Pirnar; R Israel; M Atasu
Journal:  Pediatr Radiol       Date:  1973-07

Review 5.  Punctate epiphyses: a radiological sign not a disease.

Authors:  A K Poznanski
Journal:  Pediatr Radiol       Date:  1994

6.  Calcification of cartilages, brachytelephalangy and peripheral pulmonary stenosis. Confirmation of the Keutel syndrome.

Authors:  J P Fryns; A van Fleteren; P Mattelaer; H van den Berghe
Journal:  Eur J Pediatr       Date:  1984-08       Impact factor: 3.183

7.  Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive form.

Authors:  P Maroteaux
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

Review 8.  The Keutel syndrome. Report of a case and review of the literature.

Authors:  F Ziereisen; C De Munter; N Perlmutter
Journal:  Pediatr Radiol       Date:  1993

9.  Premature tracheobronchial, laryngeal and costochondral cartilage calcification in children.

Authors:  M C Haddad; H S Sharif; M S Jared; B M Sammak; M S al Shahed
Journal:  Clin Radiol       Date:  1993-01       Impact factor: 2.350

10.  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 in total
  3 in total

1.  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

2.  Premature osteoarthritis of the knee associated with cartilage hypertrophy and phalangeal dysgenesis.

Authors:  E M J Vital; C W Hutton; P M Hughes
Journal:  Skeletal Radiol       Date:  2004-11-20       Impact factor: 2.199

Review 3.  From variome to phenome: Pathogenesis, diagnosis and management of ectopic mineralization disorders.

Authors:  Eva Yg De Vilder; Olivier M Vanakker
Journal:  World J Clin Cases       Date:  2015-07-16       Impact factor: 1.337

  3 in total

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