View source for Medicine:Orofaciodigital syndrome

{{Infobox medical condition (new)
| name            = {{PAGENAME}}
| synonyms        = Orofaciodigital syndrome
| image           = Oral-Facial-Digital Syndrome 5.jpg
| alt             = 
| caption         = Tongue in orofaciodigital syndrome
| pronounce       =
| field           =
| symptoms        =
| complications   =
| onset           =
| duration        =
| types           =
| causes          =
| risks           =
| diagnosis       =
| differential    =
| prevention      =
| treatment       =
| medication      =
| prognosis       =
| frequency       =
| deaths          =
}}
'''Orofaciodigital syndrome''' or '''oral-facial-digital syndrome''' is a group of at least 13 related conditions that affect the development of the [[Biology:Human mouth|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).<ref>{{Cite web|url=http://ghr.nlm.nih.gov/condition/oral-facial-digital-syndrome|title=Oral-facial-digital syndrome - Genetics Home Reference}}</ref>
__TOC__
== Type ==
The different types are:s<ref>{{Cite web|url=https://www.rarediseases.org/rare-disease-information/rare-diseases/byID/531/viewAbstract|title=National Organization for Rare Disorders|access-date=2015-03-02|archive-url=https://web.archive.org/web/20140816023542/http://rarediseases.org/rare-disease-information/rare-diseases/byID/531/viewAbstract|archive-date=2014-08-16|url-status=dead}}</ref>
* Type I, [[Medicine:Orofaciodigital syndrome 1|Papillon-League-Psaume syndrome]]
* Type II, Mohr syndrome<ref>{{OMIM|252100|MOHR SYNDROME}}</ref>
* Type III, [[Medicine:Sugarman syndrome|Sugarman syndrome]]
* Type IV, Baraitser-Burn syndrome<ref>{{OMIM|258860|OROFACIODIGITAL SYNDROME IV; OFD4}}</ref>
* Type V, Thurston syndrome<ref>{{OMIM|174300|OROFACIODIGITAL SYNDROME V; OFD5}}</ref>
* Type VI, Varadi-Papp syndrome<ref>{{OMIM|277170|OROFACIODIGITAL SYNDROME VI; OFD6}}</ref>
* Type VII, Whelan syndrome<ref>{{OMIM|608518|OROFACIODIGITAL SYNDROME VII; OFD7}}</ref>
* Type VIII, Oral-facial-digital syndrome, Edwards type<ref>{{OMIM|300484|OROFACIODIGITAL SYNDROME VIII; OFD8}}</ref> (not to be confused with [[Medicine:Edwards syndrome|Edwards syndrome]])
* Type IX, OFD syndrome with retinal abnormalities<ref>{{OMIM|258865|OROFACIODIGITAL SYNDROME IX; OFD9}}</ref>
* Type X, OFD with fibular aplasia<ref>{{OMIM|165590|OROFACIODIGITAL SYNDROME X; OFD10 }}</ref>
* Type XI, Gabrielli syndrome<ref>{{OMIM|612913|OROFACIODIGITAL SYNDROME XI; OFD11}}</ref>

==References==
{{Reflist}}
== External links ==
{{Medical resources
|  ICD10           = Q87.0
|  ICD9            = <!--{{ICD9|xxx}}-->
|  ICDO            =
|  OMIM            =
|  DiseasesDB      =
|  MedlinePlus     =
|  eMedicineSubj   =
|  eMedicineTopic  =
|  MeSH            =
|  GeneReviewsNBK  =
|  GeneReviewsName =
|  Orphanet        = 140997
}}
[[Category:Rare syndromes]]



{{Sourceattribution|Orofaciodigital syndrome}}