Gonadotrophin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: report of three families:Case report-Reference-Cited by-同舟云学术

Gonadotrophin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: report of three families:Case report

Published:2005-04-21 Issue:8 Volume:20 Page:2173-2178
ISSN:1460-2350
Container-title:Human Reproduction
language:en
Short-container-title:

Author:

Sato Naoko,Hasegawa Tomonobu,Hori Naoaki,Fukami Maki,Yoshimura Yasunori,Ogata Tsutomu

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynecology,Rehabilitation,Reproductive Medicine

Link

http://academic.oup.com/humrep/article-pdf/20/8/2173/9568667/dei052.pdf

Reference20 articles.

1. Aharoni A, Tal J, Paltieli Y, Porat N, Leibowitz Z and Sharf M (1989) Kallmann syndrome: a case of twin pregnancy and review of the literature. Obstet Gynecol Surv44, 491–494.

2. Buchter D, Behre HM, Kliesch S and Nieschlag E (1998) Pulsatile GnRH or human chorionic gonadotropin/human menopausal gonadotropin as effective treatment for men with hypogonadotropic hypogonadism: a review of 42 cases. Eur J Endocrinol139, 298–303.

3. Dodé C and Hardelin JP (2004) Kallmann syndrome: fibroblast growth factor signaling defect? J Mol Med82, 725–734.

4. Dodé C, Levilliers J, Dupont JM, De Paepe A, Le Du N, Soussi-Yanicostas N, Coimbra RS, Delmaghani S, Compain-Nouaille S, Baverel F et al. (2003) Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Nat Genet33, 463–465.

5. Fisher E and Scambler P (1994) Human haploinsufficiency: one for sorrow, two for joy. Nat Genet7, 5–7.

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