Oral-facial-digital syndrome
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-Leage-Psaume Syndrome).[1]
Types of oral-facial-digital syndrome[2]
- Type I, Papillon-Leage-Psaume Syndrome
- Type II, Mohr Syndrome[3]
- Type III, Sugarman Syndrome
- Type IV, Baraitser-Burn Syndrome[4]
- Type V, Thurston Syndrome[5]
- Type VI, Varadi-Papp Syndrome[6]
- Type VII, Whelan Syndrome[7]
- Type VIII, Edwards Syndrome[8]
- Type IX, OFD Syndrome with Retinal Abnormalities[9]
- Type X, OFD with Fibular Aplasia[10]
- Type XI, Gabrielli Syndrome[11]
References
- ↑ "Oral-facial-digital syndrome - Genetics Home Reference".
- ↑ "National Organization for Rare Disorders".
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) MOHR SYNDROME -252100
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) OROFACIODIGITAL SYNDROME IV; OFD4 -258860
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) OROFACIODIGITAL SYNDROME V; OFD5 -174300
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) OROFACIODIGITAL SYNDROME VI; OFD6 -277170
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) OROFACIODIGITAL SYNDROME VII; OFD7 -608518
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) OROFACIODIGITAL SYNDROME VIII; OFD8 -300484
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) OROFACIODIGITAL SYNDROME IX; OFD9 -258865
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) OROFACIODIGITAL SYNDROME X; OFD10 -165590
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) OROFACIODIGITAL SYNDROME XI; OFD11 -612913
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