Moebius and Kallmann syndromes with diabetes insipidus: a phenotype of Fibroblast Growth Factor (FGF) 8 mutation
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...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Malaysian Endocrine and Metabolic Society
2014
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| Subjects: | |
| Online Access: | http://irep.iium.edu.my/50104/ http://irep.iium.edu.my/50104/ http://irep.iium.edu.my/50104/1/98-385-1-PB.pdf |