Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome

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A rare genetic endocrine disease characterized by intrauterine growth restriction failure of an adolescent growth spurt with proportional adult short stature insulin resistance and early adulthood-onset diabetes. Minimal subluxation of the fifth metacarpal-phalangeal joint has been reported while metaphyseal dysplasia is absent. Testicular volume is low but fertility is normal. There is no evidence of primary adrenal insufficiency.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version June 2024

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