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Osteoporosis-oculocutaneous hypopigmentation syndrome

Disease definition

A rare genetic disease characterized by congenital oculocutaneous hypopigmentation, visual impairment, generalized osteoporosis with skeletal anomalies such as short stature, short neck and trunk, kyphosis, scoliosis, and platyspondyly, and dysmorphic facial features (including long philtrum, small mouth, micrognathia, and prominent ears). Moderate joint hyperelasticity and muscular hypotrophy have also been reported.

ORPHA:2786

Classification level: Disorder
  • Synonym(s):
    • Hernández-Fragoso syndrome
    • OOCHS
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: -
  • OMIM: 601220
  • UMLS: C1832592
  • MeSH: -
  • GARD: 404
  • MedDRA: -

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