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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease craniosynostosis
Comorbidity C0238402|pycnodysostosis
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PubMedID- 21968522 Since then, several mutations on unrelated patients and consanguineous families have been identified in the cathepsin k gene (ctsk), affecting osteoclast function.only two previous reports have demonstrated the presence of craniosynostosis in patients with pycnodysostosis(fleming et al., 2007; osimani et al., 2010).

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