Otopalatodigital syndrome type I

Otopalatodigital syndrome type I is a rare genetic disorder marked by the association of 

  • skeletal dysplasia
  • hearing loss
  • cleft palate
  • and a characteristic face (with hypertelorism, broad nasal root, prominent supraorbital ridges, small flat nose and downslanted palpebral fissures). 

It is a member of a group of related conditions called otopalatodigital spectrum disorders, which also includes

Article information

rID: 23291
Section: Syndromes
Synonyms or Alternate Spellings:
  • Oto-palato-digital syndrome type I
  • Otopalatodigital syndrome type 1
  • Type 1 otopalatodigital syndrome

ADVERTISEMENT: Supporters see fewer/no ads

Updating… Please wait.

 Unable to process the form. Check for errors and try again.

 Thank you for updating your details.