Paget Disease of Bone 5, Juvenile-Onset

Alternative Names

  • PDB5
  • Juvenile Paget Disease
  • JPD
  • Hyperostosis Corticalis Deformans Juvenilis
  • Hyperphosphatasemia, Chronic Congenital Idiopathic
  • Osteoectasia, Familial
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WHO-ICD-10 version:2010

Diseases of the musculoskeletal system and connective tissue

Osteopathies and chondropathies

OMIM Number

239000

Mode of Inheritance

Autosomal recessive

Gene Map Locus

8q24.12

Description

Paget disease of bone-5 is an autosomal recessive, juvenile-onset form of Paget disease, a disorder of the skeleton resulting from abnormal bone resorption and formation. Clinical manifestations include short stature, progressive long bone deformities, fractures, vertebral collapse, skull enlargement, and hyperostosis with progressive deafness. There is phenotypic variability, with some patients presenting in infancy, while others present later in childhood. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
239000.1.1EgyptMaleYesYes Recurrent fracturesNM_002546.4:c.887dupHomozygousAutosomal, RecessiveMaddirevula et al. 2018
239000.1.2EgyptMaleYesYes Recurrent fracturesNM_002546.4:c.887dupHomozygousAutosomal, RecessiveMaddirevula et al. 2018 Relative of 239000.1...
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