Congenital hypogonadotropic hypogonadism/Kallmann Syndrome is associated with statural gain in both men and women: a monocentric study.

CONCLUSIONS: CHH/KS is associated with a significant statural gain compared to the general population, mid-parental TH and same sex siblings. Greater height in CHH/KS than siblings indicates that those differences are independent of an intergenerational effect on statural gain. PMID: 31770102 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/31770102?dopt=Abstract

Source: European Journal of Endocrinology - October 31, 2019 Category: Endocrinology Authors: Maione L, Pala G, Bouvattier C, Trabado S, Papadakis G, Chanson P, Bouligand J, Pitteloud N, Dwyer AA, Maghnie M, Young J Tags: Eur J Endocrinol Source Type: research