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Eiken syndrome

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Disease definition

A rare, genetic, primary bone dysplasia syndrome characterized by multiple epiphyseal dysplasia, severely delayed ossification (mainly of the epiphyses, pubic symphysis, hands and feet), abnormal modeling of the bones in hands and feet, abnormal pelvis cartilage persistence, and mild growth retardation. Calcium, phosphate and vitamin D serum levels are typically within normal range, while parathyroid hormone serum levels are normal to slighly elevated. Oligodontia has been rarely associated.

ORPHA:79106

Classification level: Disorder

Prevalence: <1 / 1 000 000

Inheritance: Autosomal recessive

Age of onset: Infancy, Neonatal

ICD-10: M85.8

ICD-11: FB83.0Y

OMIM: 600002

UMLS: C1838779

MeSH: C564010

A summary on this disease is available in Français (2019) Español (2019) Deutsch (2019) Italiano (2019) Nederlands (2019)
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