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 (summary by Naot et al., 2014).
For discussion of genetic heterogeneity of Paget disease of bone, see 167250. [from OMIM]
- MedGen UID:
- 75678
- •Concept ID:
- C0268414
- •
- Disease or Syndrome