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.
See also reference (FX) in Slovak
rezistencia inzulínová receptor inzulínový
See also reference (FX) in English
Insulin Resistance Receptor, Insulin
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openseadragon
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