Donohue Syndrome

MeSH code information
  • Name
  • Concept
    Scope note:Rare autosomal recessive syndrome of extreme insulin resistance due to mutations in the binding domain of INSULIN RECEPTOR. Clinical features include severe intrauterine and postnatal growth restriction, characteristic dysmorphic FACIES; HIRSUTISM; VIRILIZATION; multiple endocrine abnormalities, and early death.
  • Tree numbers
    • C05.660.207.325
    • C16.131.077.313
    • C16.320.215
    • C18.452.394.750.654
    • C19.246.537
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