Orofaciodigital syndrome

Orofaciodigital syndrome or oral-facial-digital syndrome is a group of at least 13 related conditions that affect the development of the mouth, facial features, and digits in between 1 in 50,000 to 250,000 newborns with the majority of cases being type I (Papillon-League-Psaume syndrome).[1]

Orofaciodigital syndrome
Other namesOrofaciodigital syndrome
Tongue in orofaciodigital syndrome
SpecialtyRheumatology, medical genetics Edit this on Wikidata

Type

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The different types are:s[2]

References

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  1. ^ "Oral-facial-digital syndrome - Genetics Home Reference".
  2. ^ "National Organization for Rare Disorders". Archived from the original on 2014-08-16. Retrieved 2015-03-02.
  3. ^ Online Mendelian Inheritance in Man (OMIM): MOHR SYNDROME - 252100
  4. ^ Online Mendelian Inheritance in Man (OMIM): OROFACIODIGITAL SYNDROME IV; OFD4 - 258860
  5. ^ Online Mendelian Inheritance in Man (OMIM): OROFACIODIGITAL SYNDROME V; OFD5 - 174300
  6. ^ Online Mendelian Inheritance in Man (OMIM): OROFACIODIGITAL SYNDROME VI; OFD6 - 277170
  7. ^ Online Mendelian Inheritance in Man (OMIM): OROFACIODIGITAL SYNDROME VII; OFD7 - 608518
  8. ^ Online Mendelian Inheritance in Man (OMIM): OROFACIODIGITAL SYNDROME VIII; OFD8 - 300484
  9. ^ Online Mendelian Inheritance in Man (OMIM): OROFACIODIGITAL SYNDROME IX; OFD9 - 258865
  10. ^ Online Mendelian Inheritance in Man (OMIM): OROFACIODIGITAL SYNDROME X; OFD10 - 165590
  11. ^ Online Mendelian Inheritance in Man (OMIM): OROFACIODIGITAL SYNDROME XI; OFD11 - 612913
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