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Isolated growth hormone deficiency, type 4

MONDO:0032567

Also known as: growth hormone deficiency, isolated, type IV, Dwarfism of Sindh, IGHD4, ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV, Isolated Growth Hormone Deficiency, Type Ib, Isolated Growth Hormone Deficiency, Type Ib, Formerly

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Brain disorder (125) Central nervous system disorder (107) Endocrine system disorder (72) Hypogonadism (45) Isolated congenital growth hormone deficiency (36) Hereditary endocrine growth disease (24) Hypogonadotropic hypogonadism (18)
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  • Pituitary patients followed for years to uncover key outcomes

    Knowledge-focused Ongoing

    This study follows 1500 patients with pituitary gland disorders to see how they fare over time, whether treated with medication, surgery, or just monitoring. Researchers will track tumor regrowth after surgery to find clues that predict recurrence. The goal is to learn, not to te…

    Sponsor: University of Alberta • Aim: Knowledge-focused

    Last updated Jun 27, 2026 11:01 UTC

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