Literature DB >> 6787897

Familial infantile cortical hyperostosis: an update.

A H Newberg, J P Tampas.   

Abstract

In 1961, the senior author reported 11 members of one family with infantile cortical hyperostosis. Since then, 10 new cases have occurred in this family resulting in a total of 21 cases. The incidence of infantile cortical hyperostosis in this family is as common today as it was two generations ago, and there has been no diminution in the incidence. Several patients with minimal or no clinical symptoms would have gone unrecognized had it not been for the family history of the disorder. On the basis of this study, infantile cortical hyperostosis is inherited as an autosomal dominant with variable penetrance.

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Year:  1981        PMID: 6787897     DOI: 10.2214/ajr.137.1.93

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN: 0361-803X            Impact factor:   3.959


  9 in total

Review 1.  Radiographic overlap of recurrent Caffey disease and chronic recurrent multifocal osteomyelitis (CRMO) with considerations of molecular origins.

Authors:  Teresa Chapman; Sarah J Menashe; Benjamin H Taragin
Journal:  Pediatr Radiol       Date:  2019-12-23

2.  Inflammatory hyperostosis and sclerosis of the clavicle.

Authors:  A G Jurik; B N Møller
Journal:  Skeletal Radiol       Date:  1986       Impact factor: 2.199

3.  Case report 363: Infantile cortical hyperostosis (Caffey disease ICH) iliac bones, femora, tibiae and left fibula.

Authors:  R Langer; H J Kaufmann
Journal:  Skeletal Radiol       Date:  1986       Impact factor: 2.199

4.  Familial infantile cortical hyperostosis in a large Canadian family.

Authors:  A K Maclachlan; J W Gerrard; C S Houston; E J Ives
Journal:  Can Med Assoc J       Date:  1984-05-01       Impact factor: 8.262

5.  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

6.  Congenital hyperostosis in piglets: a consequence of a disorganization of the perichondrial ossification groove of Ranvier.

Authors:  B Doizé; G P Martineau
Journal:  Can J Comp Med       Date:  1984-10

7.  MRI findings in Caffey's disease.

Authors:  D G Sanders; R E Weijers
Journal:  Pediatr Radiol       Date:  1994

8.  Familial infantile cortical hyperostosis.

Authors:  L Emmery; J Timmermans; J Christens; J P Fryns
Journal:  Eur J Pediatr       Date:  1983-10       Impact factor: 3.183

9.  Infantile cortical hyperostosis and COL1A1 mutation in four generations.

Authors:  Paola Cerruti-Mainardi; Giacomo Venturi; Marianna Spunton; Elena Favaron; Michela Zignani; Sandro Provera; Bruno Dallapiccola
Journal:  Eur J Pediatr       Date:  2011-05-13       Impact factor: 3.183

  9 in total

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