Literature DB >> 7023758

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

K Fried, A Manor, M Pajewski, R Starinsky, E Vure.   

Abstract

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Year:  1981        PMID: 7023758     DOI: 10.1111/j.1399-0004.1981.tb00708.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


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  5 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.  Infantile cortical hyperostosis - a report of Saudi family.

Authors:  Muneer H ALBagshi; Heji I ALZoayed
Journal:  Sudan J Paediatr       Date:  2015

Review 3.  Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature.

Authors:  Taichi Kitaoka; Yoko Miyoshi; Noriyuki Namba; Kohji Miura; Takuo Kubota; Yasuhisa Ohata; Makoto Fujiwara; Masaki Takagi; Tomonobu Hasegawa; Harald Jüppner; Keiichi Ozono
Journal:  Eur J Pediatr       Date:  2014-01-04       Impact factor: 3.183

4.  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

5.  Professional awareness is needed to distinguish between child physical abuse from other disorders that can mimic signs of abuse (Skull base sclerosis in infant manifesting features of infantile cortical hyperostosis): a case report and review of the literature.

Authors:  Ali Al Kaissi; Gert Petje; Veerla De Brauwer; Franz Grill; Klaus Klaushofer
Journal:  Cases J       Date:  2009-02-09
  5 in total

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