Newborn with cleidocranial dysplasia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Radiology, Nuclear Medicine and imaging
Link
https://link.springer.com/content/pdf/10.1007/s00256-022-04095-5.pdf
Reference7 articles.
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.
2. Komori T. Runx2, an inducer of osteoblast and chondrocyte differentiation. Histochem Cell Biol. 2018;149:313–32.
3. 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.
4. 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.
5. Chalfant JS, Sanchez TR. Congenital clavicular pseudoarthosis-how to differentiate it from the more common clavicular fractures. Pediatr Emerg Care. 2019;35:e37–9.
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