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Additional conditions under the umbrella of congenital IGF-1 deficiencies include a documented case of a 15-year-old boy suffering from severe prenatal and postnatal growth failure, sensorineural deafness and mental retardation due to a homozygous partial deletion of the IGF-I gene [41] as well as IGF1R genes defects [42]

Jossy Onwude, MD Jul 3, 2026 14 min read Hexarelin: The Cardioprotective Growth Hormone Peptide That Mainstream Providers Overlook Editorial Team Jul 2, 2026 14 min read Best-in-class care is a click away Find everything and everyone you need to reach your metabolic health goals, in one place

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[DOI] [PMC free article] [PubMed] [Google Scholar] 75.Fond G, Lanon C, Korchia T, Auquier P, Boyer L

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