Orphanet: S ndrome de Marshall Smith

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Marshall-Smith syndrome

Disease definition

Marshall-Smith syndrome is a rare genetic disease characterized by tall stature and advanced bone age at birth.


Classification level: Disorder
  • Synonym(s):
    • Accelerated skeletal maturation-facial dysmorphism-failure to thrive syndrome
  • Prevalence: <1 / 1 000 000
  • Inheritance: Unknown 
  • Age of onset: Infancy, Neonatal
  • ICD-10: Q87.3
  • OMIM: 602535
  • UMLS: C0265211
  • MeSH: C536026
  • GARD: 6985
  • MedDRA: -
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