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Gómez-López-Hernández syndrome

Disease definition

Lopez-Hernandez syndrome, which may be classified among the neurocutaneous syndromes, associates abnormalities of the cerebellum (rhombencephalosynapsis), cranial nerves (trigeminal anesthesia), and scalp (alopecia). It has been reported in 11 individuals so far. Other features observed in patients were craniosynostosis, midfacial hypoplasia, bilateral corneal opacities, low-set ears, short stature, moderate intellectual impairment and ataxia. Hyperactivity, depression, self-injurious behaviour and bipolar disorder have also been reported.

ORPHA:1532

Classification level: Disorder
  • Synonym(s):
    • Cerebellotrigeminal-dermal dysplasia syndrome
    • Craniosynostosis-alopecia-brain defect syndrome
  • Prevalence: <1 / 1 000 000
  • Inheritance: Not applicable 
  • Age of onset: Neonatal
  • ICD-10: Q07.8
  • OMIM: 601853
  • UMLS: C0795959
  • MeSH: -
  • GARD: 1586  229
  • MedDRA: -

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