Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Moebius syndrome is a very rare congenital cranial dysinnervation disorder characterized by complete or incomplete facial paralysis in association with bilateral palsy of the abducens nerve causing impairment of ocular abduction. The syndrome also includes various other congenital anomalies.
Features include always present findings: Hand clenching; and common findings: Abnormality of the dentition, Delayed speech and language development, and Micrognathia. 51 total HPO annotations.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Brain and nerves | 9 | Mild intellectual disability, Clumsiness, Dysarthria |
Phenotype severity distribution: 1 always present feature, 3 common features.
Estimated prevalence: 1-9 in 100,000 (Uncommon).
1 clinical trial registered, 1 recruiting. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.
43 publications have been identified in PubMed for Mobius syndrome. Research spans Case Report / Case Series (44%), Review / Meta-Analysis (26%), and Clinical Trial Publication (12%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 19 | 44% |
Data assembled from 6 of 12 sources · Last updated Sep 20, 2026, 2:11 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Mobius syndrome
Arms and legs
5 |
Lower limb undergrowth, Split hand, Radial deviation of finger |
Muscles | 2 | Congenital fibrosis of extraocular muscles, Joint stiffness present at birth (arthrogryposis multiplex congenita) |
Digestive system | 2 | Feeding difficulties in infancy, Difficulty swallowing (dysphagia) |
Head and neck | 2 | Facial diplegia, High palate |
Bones and joints | 2 | Aplasia/Hypoplasia involving the metacarpal bones, Abnormal pelvic girdle bone morphology |
Hormones | 1 | Hypogonadotropic hypogonadism |
Pregnancy and birth | 1 | Congenital fibrosis of extraocular muscles |
Voice | 1 | Abnormality of the voice |
Skin | 1 | Abnormal nail morphology |
Lungs and breathing | 1 | Respiratory distress |
Research summaries |
11 |
26% |
Clinical study results | 5 | 12% |
Disease patterns and progression | 4 | 9% |
Laboratory research | 3 | 7% |
Other research | 1 | 2% |
Gonçalves CP (2026). [PMID: 41658652](https://pubmed.ncbi.nlm.nih.gov/41658652/). *Cureus*. [Case Report / Case Series]
Gamio S (2026). [PMID: 42212635](https://pubmed.ncbi.nlm.nih.gov/42212635/). *Strabismus*. [Case Report / Case Series]
Aufderheide K (2026). [PMID: 41870107](https://pubmed.ncbi.nlm.nih.gov/41870107/). *International ophthalmology clinics*. [Review / Meta-Analysis]
Nguyen CT (2026). [PMID: 41948882](https://pubmed.ncbi.nlm.nih.gov/41948882/). *Head Neck*. [Case Report / Case Series]
Telich-Tarriba JE (2026). [PMID: 41275539](https://pubmed.ncbi.nlm.nih.gov/41275539/). *Journal of plastic, reconstructive & aesthetic surgery : JPRAS*. [Review / Meta-Analysis]
de Groot-van der Mooren MD (2026). [PMID: 41569079](https://pubmed.ncbi.nlm.nih.gov/41569079/). *Nederlands tijdschrift voor geneeskunde*. [Case Report / Case Series]
He M (2025). [PMID: 39834316](https://pubmed.ncbi.nlm.nih.gov/39834316/). *Facial plastic surgery & aesthetic medicine*. [Clinical Trial Publication]
Fukumoto-Inukai KA (2025). [PMID: 40100160](https://pubmed.ncbi.nlm.nih.gov/40100160/). *Plastic and reconstructive surgery*. [Clinical Trial Publication]
Molinari S (2025). [PMID: 39846147](https://pubmed.ncbi.nlm.nih.gov/39846147/). *Journal of pediatric endocrinology & metabolism : JPEM*. [Review / Meta-Analysis]
Kuzucu P (2025). [PMID: 41174533](https://pubmed.ncbi.nlm.nih.gov/41174533/). *BMC pediatrics*. [Review / Meta-Analysis]