Moebius and Kallmann syndromes with diabetes insipidus: a phenotype of Fibroblast Growth Factor (FGF) 8 mutation

• Main Authors: Omar , Ahmad Marzuki, Shahar, Mohammad Arif, Abd Wahab, Norasyikin, Mustafa, Norlaila, Sukor, Norlela, Kamaruddin, Nor Azmi
• Format: Article
• Language: English
• Published: Malaysian Endocrine and Metabolic Society 2014
• Subjects: R Medicine (General); RC Internal medicine
• Online Access: http://irep.iium.edu.my/50104/1/98-385-1-PB.pdf; http://irep.iium.edu.my/50104/; http://www.jmems.org/index.php/jmems/article/viewFile/98/87

Moebius syndrome is a rare congenital condition typically characterised by congenital facial and abducens nerve palsies. Dysfunction of other cranial nerves, malformations of orofacial structures, and limb anomalies may also be present. The aetiology is not well understood, but may relate to chro...