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Editorial
. 2022 Dec;51(12):2351-2352.
doi: 10.1007/s00256-022-04095-5. Epub 2022 Jun 21.

Newborn with cleidocranial dysplasia

Roberto Franceschi  1 , Giovanna Stringari  2 , Fiorenza Soli  3 , Annalisa Pedrolli  4 , Evelina Maines  4
Affiliations
Editorial

Newborn with cleidocranial dysplasia

Roberto Franceschi et al. Skeletal Radiol. 2022 Dec.
No abstract available

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References

    1. Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, et al. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia. Cell. 1997;89:773–9. - DOI
    1. Komori T. Runx2, an inducer of osteoblast and chondrocyte differentiation. Histochem Cell Biol. 2018;149:313–32. - DOI
    1. Franceschi R, Maines E, Fedrizzi M, Piemontese MR, De Bonis P, Agarwal N, et al. Familial cleidocranial dysplasia misdiagnosed as rickets over three generations. Pediatr Int. 2015;57:1003–6. - DOI
    1. Kim JH, Kim SJ, Kim HH, Kim JK. Sporadic cleidocranial dysplasia in a newborn: a 4-year follow-up study. Neonatal Med. 2020;27:192–6. - DOI
    1. Chalfant JS, Sanchez TR. Congenital clavicular pseudoarthosis-how to differentiate it from the more common clavicular fractures. Pediatr Emerg Care. 2019;35:e37–9. - DOI

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