Summarized by Plex Health
Last Updated: 09 May 2022

Otopalatodigital syndrome type 1 is a disorder mostly entailing irregularities in skeletal advancement. It is a member of a group of associated conditions called otopalatodigital spectrum disorders, which additionally consists of otopalatodigital syndrome type 2, frontometaphyseal dysplasia, Melnick-Needles syndrome, and terminal bony dysplasia. Otopalatodigital syndrome type 1 is usually the mildest of the otopalatodigital spectrum disorders. Affected individuals additionally have hearing loss. Babies with otopalatodigital syndrome type 1 may be birthed with an opening in the roof of the mouth. Individuals with this problem often have less teeth than normal. People with otopalatodigital syndrome type 1 might be somewhat shorter than other members of their family. Females with otopalatodigital syndrome type 1 typically have more variable symptoms and signs contrasted to affected men, with females normally having fewer signs and symptoms.

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions

** If you believe that content on the Plex is summarised improperly, please, contact us, and we will get rid of it quickly; please, send an email with a brief explanation.

*** If you want us to remove all links leading to your domain from Plex.page and never use your website as a source of the "Online Knowledge", please contact us using a corporate email and we will remove everything in 10 business days.


Plex Page is a Biology & Health Sciences "Online Knowledge Base," where a machine summarizes all the summaries.