The 20 Best Orofaciodigital Syndrome 4 Doctors in Qatar

Find the Top Orofaciodigital Syndrome 4 Experts and Specialists

Last Updated: 04/28/2026

Save doctors for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Already have a doctor?
Find A Second Opinion

MediFind found 1 doctor with experience in Orofaciodigital Syndrome 4 near Qatar. Of these, 1 are Distinguished.

Location
LocationClose
1 provider found
    Distinguished in Orofaciodigital Syndrome 4
    Distinguished in Orofaciodigital Syndrome 4
    Research Branch, 
    Doha, DA, QA 

    Shoaib Nawaz practices practicing medicine in Doha, Qatar. Mr. Nawaz is rated as a Distinguished expert by MediFind in the treatment of Orofaciodigital Syndrome 4. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Orofaciodigital Syndrome 4, Dyggve-Melchior-Clausen Syndrome, Syndactyly Cenani Lenz Type, and Symphalangism Distal.

    Learn about our expert tiers
    While we make every effort to provide the best results possible, data is currently limited outside of the United States. Doctors listed may include both clinicians and researchers, and individuals relocate frequently. We recommend contacting doctors directly to confirm their location and areas of focus. Contact information is provided when available. Learn more about our expert tiers.
    Showing 1-1 of 1

    Last Updated: 04/28/2026

    What is the definition of Orofaciodigital Syndrome 4?

    Orofaciodigital syndrome 4 is one of a group of related conditions that affect the development of the oral cavity (the mouth and teeth), facial features, and digits (fingers and toes). Specific features, while variable, commonly include non-cancerous tumors (hamartomas) of the tongue, polydactyly of the hands and feet, severe clubfoot, and shortening and bowing of the middle portion of the lower leg (mesomelic limb shortening with tibial dysplasia). Orofaciodigital syndrome 4 is inherited in an autosomal recessive fashion. The condition appears to be caused by genetic changes in the tectonic family member 3 gene (TCTN3).