Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome

Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome(来自ICD-11)

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome An important gene associated with Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome is LRP5 (LDL Receptor Related Protein 5). Affiliated tissues include bone, and related phenotypes are macrocephaly and hypertelorism

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