Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?
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BORIS DOI
Date of Publication
January 2015
Publication Type
Article
Division/Institute
Contributor
Romani, Marta | |
Mancini, Francesca | |
Micalizzi, Alessia | |
Poretti, Andrea | |
Miccinilli, Elide | |
Accorsi, Patrizia | |
Avola, Emanuela | |
Bertini, Enrico | |
Borgatti, Renato | |
Romaniello, Romina | |
Ceylaner, Serdar | |
Coppola, Giangennaro | |
D'Arrigo, Stefano | |
Giordano, Lucio | |
Janecke, Andreas R | |
Lituania, Mario | |
Ludwig, Kathrin | |
Martorell, Loreto | |
Mazza, Tommaso | |
Odent, Sylvie | |
Pinelli, Lorenzo | |
Poo, Pilar | |
Santucci, Margherita | |
Signorini, Sabrina | |
Simonati, Alessandro | |
Spiegel, Ronen | |
Stanzial, Franco | |
Tabarki, Brahim | |
Wolf, Nicole I | |
Zibordi, Federica | |
Boltshauser, Eugen | |
Valente, Enza Maria |
Subject(s)
Series
Human genetics
ISSN or ISBN (if monograph)
0340-6717
Publisher
Springer
Language
English
Publisher DOI
PubMed ID
25407461
Description
Oral-facial-digital type VI syndrome (OFDVI) is a rare phenotype of Joubert syndrome (JS). Recently, C5orf42 was suggested as the major OFDVI gene, being mutated in 9 of 11 families (82 %). We sequenced C5orf42 in 313 JS probands and identified mutations in 28 (8.9 %), most with a phenotype of pure JS. Only 2 out of 17 OFDVI patients (11.7 %) were mutated. A comparison of mutated vs. non-mutated OFDVI patients showed that preaxial and mesoaxial polydactyly, hypothalamic hamartoma and other congenital defects may predict C5orf42 mutations, while tongue hamartomas are more common in negative patients.
File(s)
| File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
|---|---|---|---|---|---|---|---|
| art%3A10.1007%2Fs00439-014-1508-3.pdf | text | Adobe PDF | 353.85 KB | Attribution (CC BY 4.0) | published |