Literature DB >> 6357801

Familial infantile cortical hyperostosis.

L Emmery, J Timmermans, J Christens, J P Fryns.   

Abstract

Infantile cortical hyperostosis occurred in three generations of a family affecting eight different members. As confirmed in this family, Caffey disease is an autosomal dominant disorder of unknown etiology, with incomplete penetrance and variable expression.

Entities:  

Mesh：

Year:  1983        PMID： 6357801     DOI： 10.1007/bf00445672

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


  14 in total

1.  Familial infantile cortical hyperostosis.

Authors:  J W GERRARD; G H HOLMAN; A A GORMAN; I H MORROW
Journal:  J Pediatr       Date:  1961-10       Impact factor: 4.406

2.  Infantile cortical hyperostosis: an inquiry into its familial aspects.

Authors:  F W VAN BUSKIRK; J P TAMPAS; O S PETERSON
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1961-04

Review 3.  Infantile cortical hyperostosis. Review of the literature and report of a case without mandibular involvement.

Authors:  A K Wilson
Journal:  Clin Orthop Relat Res       Date:  1969 Jan-Feb       Impact factor: 4.176

4.  Infantile cortical hyperostosis. Follow-up of 29 cases.

Authors:  A Finsterbush; M Rang
Journal:  Acta Orthop Scand       Date:  1975-11

5.  Case report 139. Infantile cortical hyperostosis (Caffey disease).

Authors:  J M Katz; J A Kirkpatrick; N Papanicolaou; P Desai
Journal:  Skeletal Radiol       Date:  1981       Impact factor: 2.199

6.  Hitherto undescribed characteristics of the pathology of infantile cortical hyperostosis (Caffey's disease).

Authors:  S L EVERSOLE; G H HOLMAN; R A ROBINSON
Journal:  Bull Johns Hopkins Hosp       Date:  1957-08

7.  Familial infantile cortical hyperostosis: an update.

Authors:  A H Newberg; J P Tampas
Journal:  AJR Am J Roentgenol       Date:  1981-07       Impact factor: 3.959

8.  Caffey's disease revisited. Further evidence for autosomal dominant inheritance with incomplete penetrance.

Authors:  R A Saul; W H Lee; R E Stevenson
Journal:  Am J Dis Child       Date:  1982-01

9.  Late manifestations of infantile cortical hyperostosis (Caffey's disease).

Authors:  M Pajewski; E Vure
Journal:  Br J Radiol       Date:  1967-02       Impact factor: 3.039

10.  Autosomal dominant inheritance with incomplete penetrance of Caffey disease (infantile cortical hyperostosis).

Authors:  K Fried; A Manor; M Pajewski; R Starinsky; E Vure
Journal:  Clin Genet       Date:  1981-04       Impact factor: 4.438
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  1 in total

1.  The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease).

Authors:  Tae-Joon Cho; Hyuk Ju Moon; Dae-Yeon Cho; Moon Seok Park; Dong Yeon Lee; Won Joon Yoo; Chin Youb Chung; In Ho Choi
Journal:  J Hum Genet       Date:  2008-08-13       Impact factor: 3.172
  1 in total

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