 Donohue Syndrome
"Donohue Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D056731
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| MeSH Number(s) |
C05.660.207.325 C16.131.077.313 C16.320.215 C18.452.394.750.654 C19.246.537
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| Concept/Terms |
Rabson-Mendenhall Syndrome- Rabson-Mendenhall Syndrome
- Rabson Mendenhall Syndrome
- Syndrome, Rabson-Mendenhall
- Mendenhall Syndrome
- Syndrome, Mendenhall
- Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities
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Below are MeSH descriptors whose meaning is more general than "Donohue Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Donohue Syndrome".
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Below are the most recent publications written about "Donohue Syndrome" by people in Profiles.
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