The fragile-X syndrome is the most common cause of inherited mental retardation and it is associated with the FMR1 gene on X chromosome. The origin of anatomic anomalies of maxillo-facial complex is still discussed in literature. The authors describe the syndrome and report a clinical case.

Muzzi, F., Santini, F., Romanini, G., Bartuli, F.n., Arcuri, C. (2010). Fragile-X syndrome: genetic aspects and stomatologic evaluations. ORAL & IMPLANTOLOGY, 3(3), 38-44.

Fragile-X syndrome: genetic aspects and stomatologic evaluations

Bartuli, F N;Arcuri, C
2010-07-01

Abstract

The fragile-X syndrome is the most common cause of inherited mental retardation and it is associated with the FMR1 gene on X chromosome. The origin of anatomic anomalies of maxillo-facial complex is still discussed in literature. The authors describe the syndrome and report a clinical case.
lug-2010
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/28 - MALATTIE ODONTOSTOMATOLOGICHE
English
FMRP protein; Martin-Bell syndrome; fragile-X syndrome
Muzzi, F., Santini, F., Romanini, G., Bartuli, F.n., Arcuri, C. (2010). Fragile-X syndrome: genetic aspects and stomatologic evaluations. ORAL & IMPLANTOLOGY, 3(3), 38-44.
Muzzi, F; Santini, F; Romanini, G; Bartuli, Fn; Arcuri, C
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/233015
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