Snyder-Robinson syndrome: differential diagnosis of osteogenesis imperfecta

Author:

Valera Ribera C,Martinez-Ferrer À,Flores Fernández E,Vázquez Gómez I,Orenes Vera A,Valls Pascual E,Ybáñez García D,Alegre Sancho JJ

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology, Diabetes and Metabolism

Reference7 articles.

1. Schwartz CE, Peron A, Kutler MJ (2013) Snyder-Robinson syndrome. 2013 Jun 27 [Updated 2020 Feb 13]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021.

2. Murray-Stewart T, Dunworth M, Foley JR, Schwartz CE, Casero RA Jr (2018) Polyamine homeostasis in Snyder-Robinson syndrome. Med Sci (Basel) 6(4):112

3. Larcher L, Norris JW, Lejeune E, Buratti J, Mignot C, Garel C, Keren B, Schwartz CE, Whalen S (2020) The complete loss of function of the SMS gene results in a severe form of Snyder-Robinson syndrome. Eur J Med Genet. 63(4):103777

4. Ward L, Glorieux F, Rauch F (2004) Osteogenesis imperfecta. Canadian Paediatric Surveillance Program [Internet]. Available from: https://www.cpsp.cps.ca/uploads/studies/osteogenesis-imperfecta-protocol.pdf.

5. Vannala V, Palaian S, Shankar PR (2020) Therapeutic dimensions of bisphosphonates: a clinical update. Int J Prev Med 11:166

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