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Clinical and molecular features of idiopathic hypogonadotropic hypogonadism in Taiwan: A single center experience.
Cho CY, Tsai WY, Lee CT, Liu SY, Huang SY, Chien YH, Hwu WL, Lee NC, Tung YC. Cho CY, et al. J Formos Med Assoc. 2022 Jan;121(1 Pt 1):218-226. doi: 10.1016/j.jfma.2021.03.010. Epub 2021 Mar 26. J Formos Med Assoc. 2022. PMID: 33775534 Free article.
BACKGROUND: Idiopathic (isolated) hypogonadotropic hypogonadism (IHH) is a rare disease that can be classified as Kallmann syndrome (KS) or normosmic IHH (nIHH). ...
BACKGROUND: Idiopathic (isolated) hypogonadotropic hypogonadism (IHH) is a rare disease that can be classified as Kallm …
Pathology or normal variant: what constitutes a delay in puberty?
Villanueva C, Argente J. Villanueva C, et al. Horm Res Paediatr. 2014;82(4):213-21. doi: 10.1159/000362600. Epub 2014 Jul 7. Horm Res Paediatr. 2014. PMID: 25011467 Free article. Review.
Three major groups of etiopathogeneses are described: (1) hypogonadotropic hypogonadism, (2) hypergonadotropic hypogonadism, and (3) constitutional delay of puberty (CDP) - the most common cause of delayed puberty in boys. The differential diagnosis between CDP and isolated …
Three major groups of etiopathogeneses are described: (1) hypogonadotropic hypogonadism, (2) hypergonadotropic hypogonadism, and (3) constit …
Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism.
Zhou C, Niu Y, Xu H, Li Z, Wang T, Yang W, Wang S, Wang DW, Liu J. Zhou C, et al. Fertil Steril. 2018 Aug;110(3):486-495.e5. doi: 10.1016/j.fertnstert.2018.04.010. Fertil Steril. 2018. PMID: 30098700 Free article.
OBJECTIVE: To investigate the mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism (IHH) and discover new pathogenic genes that cause IHH. ...
OBJECTIVE: To investigate the mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic …
ART outcomes of patients in women with Isolated Hypogonadotropic Hypogonadism: a retrospective study in China.
Xu W, Li R, Qiao J. Xu W, et al. BMC Pregnancy Childbirth. 2023 Apr 14;23(1):255. doi: 10.1186/s12884-023-05579-5. BMC Pregnancy Childbirth. 2023. PMID: 37059970 Free PMC article.
BACKGROUND: Isolated Hypogonadotropic Hypogonadism (IHH) is a rare reproductive disorder caused by the dysfunction of the gonadotropin-releasing hormone axis. ...
BACKGROUND: Isolated Hypogonadotropic Hypogonadism (IHH) is a rare reproductive disorder caused by the dysfunction of t …
Isolated hypogonadotropic hypogonadism in adolescence: Do we need to measure the pituitary, stalk or other imaging markers? A retrospective magnetic resonance imaging study.
Ayaz E, Yıldırım R, Çelebi C, Özalkak Ş. Ayaz E, et al. Turk J Pediatr. 2023;65(3):445-455. doi: 10.24953/turkjped.2022.1095. Turk J Pediatr. 2023. PMID: 37395964 Free article.
Our aim was to compare the size of the pituitary gland, stalk and other previously described imaging tools in patients with isolated hypogonadotropic hypogonadism (HH) versus adolescents with a normal pituitary gland. ...
Our aim was to compare the size of the pituitary gland, stalk and other previously described imaging tools in patients with isolated …
A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.
Wang X, Chen D, Zhao Y, Men M, Chen Z, Jiang F, Zheng R, Stamou MI, Plummer L, Balasubramanian R, Li JD. Wang X, et al. Hum Mol Genet. 2023 May 5;32(10):1722-1729. doi: 10.1093/hmg/ddad014. Hum Mol Genet. 2023. PMID: 36694982 Free PMC article.
Isolated hypogonadotropic hypogonadism (IHH) is a rare disease with hypogonadism and infertility caused by the defects in embryonic migration of hypothalamic gonadotropin-releasing hormone (GnRH) neurons, hypothalamic GnRH secretion or GnRH signal transductio …
Isolated hypogonadotropic hypogonadism (IHH) is a rare disease with hypogonadism and infertility caused by the defects …
Clinical review: Distinguishing constitutional delay of growth and puberty from isolated hypogonadotropic hypogonadism: critical appraisal of available diagnostic tests.
Harrington J, Palmert MR. Harrington J, et al. J Clin Endocrinol Metab. 2012 Sep;97(9):3056-67. doi: 10.1210/jc.2012-1598. Epub 2012 Jun 20. J Clin Endocrinol Metab. 2012. PMID: 22723321 Review.
Specifically, clinicians often cannot distinguish constitutional delay of growth and puberty (CDGP) from isolated hypogonadotropic hypogonadism (IHH), with definitive diagnosis of IHH awaiting lack of spontaneous puberty by age 18 yr. ...
Specifically, clinicians often cannot distinguish constitutional delay of growth and puberty (CDGP) from isolated hypogonadotropic …
Spectrum of phenotype and genotype of congenital isolated hypogonadotropic hypogonadism in Asian Indians.
Nair S, Jadhav S, Lila A, Jagtap V, Bukan A, Pandit R, Ekbote A, Dharmalingam M, Kumar P, Kalra P, Gandhi P, Walia R, Sankhe S, Raghavan V, Shivane V, Menon P, Bandgar T, Shah N. Nair S, et al. Clin Endocrinol (Oxf). 2016 Jul;85(1):100-9. doi: 10.1111/cen.13009. Epub 2016 Feb 12. Clin Endocrinol (Oxf). 2016. PMID: 26708526
BACKGROUND: Congenital isolated hypogonadotropic hypogonadism (IHH) is caused due to defect in GnRH neuronal development, migration and action. ...
BACKGROUND: Congenital isolated hypogonadotropic hypogonadism (IHH) is caused due to defect in GnRH neuronal developmen …
Reproductive Phenotypes and Genotypes in Men With IHH.
Dwyer AA, Stamou MI, Anghel E, Hornstein S, Chen D, Salnikov KB, McDonald IR, Plummer L, Seminara SB, Balasubramanian R. Dwyer AA, et al. J Clin Endocrinol Metab. 2023 Mar 10;108(4):897-908. doi: 10.1210/clinem/dgac615. J Clin Endocrinol Metab. 2023. PMID: 36268624 Free PMC article.
CONTEXT: Isolated hypogonadotropic hypogonadism (IHH) is phenotypically and genetically heterogeneous. ...
CONTEXT: Isolated hypogonadotropic hypogonadism (IHH) is phenotypically and genetically heterogeneous. ...
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH).
Bonomi M, Vezzoli V, Krausz C, Guizzardi F, Vezzani S, Simoni M, Bassi I, Duminuco P, Di Iorgi N, Giavoli C, Pizzocaro A, Russo G, Moro M, Fatti L, Ferlin A, Mazzanti L, Zatelli MC, Cannavò S, Isidori AM, Pincelli AI, Prodam F, Mancini A, Limone P, Tanda ML, Gaudino R, Salerno M, Francesca P, Maghnie M, Maggi M, Persani L; Italian Network on Central Hypogonadism; Italian Network on Central Hypogonadism (NICe group). Bonomi M, et al. Eur J Endocrinol. 2018 Jan;178(1):23-32. doi: 10.1530/EJE-17-0065. Epub 2017 Sep 7. Eur J Endocrinol. 2018. PMID: 28882981 Free article.
OBJECTIVE: Isolated hypogonadotropic hypogonadism (IHH) is a rare disorder with pubertal delay, normal (normoosmic-IHH, nIHH) or defective sense of smell (Kallmann syndrome, KS). ...
OBJECTIVE: Isolated hypogonadotropic hypogonadism (IHH) is a rare disorder with pubertal delay, normal (normoosmic-IHH, …
58 results