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Congenital GHD is present at birth (or shortly after) and is usually caused by genetic abnormalities or malformations in the hypothalamus or pituitary gland
Ik M, Beydemir , Ylmaz A, Naldan ME, Aslan HE, Glin
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What can we conclude from this study
Its proposed mechanism is to stimulate lipolysis (the breakdown of stored fat) and to inhibit lipogenesis (the formation of new fat), apparently through -adrenergic-related pathways, while unlike full-length GH not raising IGF-1 and not impairing glucose tolerance [1] [5]
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