Genetics of congenital hypogonadotropic hypogonadism in Denmark

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Genetics of congenital hypogonadotropic hypogonadism in Denmark. / Tommiska, Johanna; Känsäkoski, Johanna; Christiansen, Peter; Jørgensen, Niels; Lawaetz, Jacob Gerner; Juul, Anders; Raivio, Taneli.

I: European Journal of Medical Genetics, Bind 57, Nr. 7, 07.2014, s. 345-348.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Tommiska, J, Känsäkoski, J, Christiansen, P, Jørgensen, N, Lawaetz, JG, Juul, A & Raivio, T 2014, 'Genetics of congenital hypogonadotropic hypogonadism in Denmark', European Journal of Medical Genetics, bind 57, nr. 7, s. 345-348. https://doi.org/10.1016/j.ejmg.2014.04.002

APA

Tommiska, J., Känsäkoski, J., Christiansen, P., Jørgensen, N., Lawaetz, J. G., Juul, A., & Raivio, T. (2014). Genetics of congenital hypogonadotropic hypogonadism in Denmark. European Journal of Medical Genetics, 57(7), 345-348. https://doi.org/10.1016/j.ejmg.2014.04.002

Vancouver

Tommiska J, Känsäkoski J, Christiansen P, Jørgensen N, Lawaetz JG, Juul A o.a. Genetics of congenital hypogonadotropic hypogonadism in Denmark. European Journal of Medical Genetics. 2014 jul.;57(7):345-348. https://doi.org/10.1016/j.ejmg.2014.04.002

Author

Tommiska, Johanna ; Känsäkoski, Johanna ; Christiansen, Peter ; Jørgensen, Niels ; Lawaetz, Jacob Gerner ; Juul, Anders ; Raivio, Taneli. / Genetics of congenital hypogonadotropic hypogonadism in Denmark. I: European Journal of Medical Genetics. 2014 ; Bind 57, Nr. 7. s. 345-348.

Bibtex

@article{d5aa84ae293c4d87a1882a50b202f6d9,
title = "Genetics of congenital hypogonadotropic hypogonadism in Denmark",
abstract = "Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder characterized by incomplete/absent puberty caused by deficiency or defective action of gonadotropin-releasing hormone (GnRH). The phenotypic features of patients with CHH vary from genital hypoplasia and absent puberty to reversal of HH later in life. We examined the genetics and clinical features of CHH in Denmark. Forty-one male patients were screened for mutations in KAL1, FGFR1, FGF8, PROK2, PROKR2, GNRHR, TAC3, TACR3, and KISS1R. CHD7 was screened in two patients with hearing loss. In 12 patients, a molecular genetic cause for CHH was found. Four patients had mutations in KAL1 (C105VfsX13, C53X, ex5-8del, R257X), and five in FGFR1 (G97S, R209C, A512V, R646W, and c.1614C>T, (p.I538I), predicted to affect splicing). All 9 had severe HH (cryptorchidism and/or micropenis), and 2 had cleft lip/palate. One patient with a previously reported homozygous R262Q mutation in GNRHR displayed fascinating temporal variation in his phenotype. Two patients with hearing loss had CHD7 mutations (c.7832_7841del (p.K2611MfsX25) and c.2443-2A>C), confirming that CHH patients with CHARGE syndrome-associated features should be screened for mutations in CHD7.",
keywords = "DNA Helicases, DNA-Binding Proteins, Denmark, Extracellular Matrix Proteins, Genetic Diseases, Inborn, Humans, Hypogonadism, Male, Mutation, Nerve Tissue Proteins, Receptor, Fibroblast Growth Factor, Type 1, Receptors, LHRH",
author = "Johanna Tommiska and Johanna K{\"a}ns{\"a}koski and Peter Christiansen and Niels J{\o}rgensen and Lawaetz, {Jacob Gerner} and Anders Juul and Taneli Raivio",
note = "Copyright {\textcopyright} 2014 Elsevier Masson SAS. All rights reserved.",
year = "2014",
month = jul,
doi = "10.1016/j.ejmg.2014.04.002",
language = "English",
volume = "57",
pages = "345--348",
journal = "European Journal of Medical Genetics",
issn = "1769-7212",
publisher = "Elsevier Masson",
number = "7",

}

RIS

TY - JOUR

T1 - Genetics of congenital hypogonadotropic hypogonadism in Denmark

AU - Tommiska, Johanna

AU - Känsäkoski, Johanna

AU - Christiansen, Peter

AU - Jørgensen, Niels

AU - Lawaetz, Jacob Gerner

AU - Juul, Anders

AU - Raivio, Taneli

N1 - Copyright © 2014 Elsevier Masson SAS. All rights reserved.

PY - 2014/7

Y1 - 2014/7

N2 - Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder characterized by incomplete/absent puberty caused by deficiency or defective action of gonadotropin-releasing hormone (GnRH). The phenotypic features of patients with CHH vary from genital hypoplasia and absent puberty to reversal of HH later in life. We examined the genetics and clinical features of CHH in Denmark. Forty-one male patients were screened for mutations in KAL1, FGFR1, FGF8, PROK2, PROKR2, GNRHR, TAC3, TACR3, and KISS1R. CHD7 was screened in two patients with hearing loss. In 12 patients, a molecular genetic cause for CHH was found. Four patients had mutations in KAL1 (C105VfsX13, C53X, ex5-8del, R257X), and five in FGFR1 (G97S, R209C, A512V, R646W, and c.1614C>T, (p.I538I), predicted to affect splicing). All 9 had severe HH (cryptorchidism and/or micropenis), and 2 had cleft lip/palate. One patient with a previously reported homozygous R262Q mutation in GNRHR displayed fascinating temporal variation in his phenotype. Two patients with hearing loss had CHD7 mutations (c.7832_7841del (p.K2611MfsX25) and c.2443-2A>C), confirming that CHH patients with CHARGE syndrome-associated features should be screened for mutations in CHD7.

AB - Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder characterized by incomplete/absent puberty caused by deficiency or defective action of gonadotropin-releasing hormone (GnRH). The phenotypic features of patients with CHH vary from genital hypoplasia and absent puberty to reversal of HH later in life. We examined the genetics and clinical features of CHH in Denmark. Forty-one male patients were screened for mutations in KAL1, FGFR1, FGF8, PROK2, PROKR2, GNRHR, TAC3, TACR3, and KISS1R. CHD7 was screened in two patients with hearing loss. In 12 patients, a molecular genetic cause for CHH was found. Four patients had mutations in KAL1 (C105VfsX13, C53X, ex5-8del, R257X), and five in FGFR1 (G97S, R209C, A512V, R646W, and c.1614C>T, (p.I538I), predicted to affect splicing). All 9 had severe HH (cryptorchidism and/or micropenis), and 2 had cleft lip/palate. One patient with a previously reported homozygous R262Q mutation in GNRHR displayed fascinating temporal variation in his phenotype. Two patients with hearing loss had CHD7 mutations (c.7832_7841del (p.K2611MfsX25) and c.2443-2A>C), confirming that CHH patients with CHARGE syndrome-associated features should be screened for mutations in CHD7.

KW - DNA Helicases

KW - DNA-Binding Proteins

KW - Denmark

KW - Extracellular Matrix Proteins

KW - Genetic Diseases, Inborn

KW - Humans

KW - Hypogonadism

KW - Male

KW - Mutation

KW - Nerve Tissue Proteins

KW - Receptor, Fibroblast Growth Factor, Type 1

KW - Receptors, LHRH

U2 - 10.1016/j.ejmg.2014.04.002

DO - 10.1016/j.ejmg.2014.04.002

M3 - Journal article

C2 - 24732674

VL - 57

SP - 345

EP - 348

JO - European Journal of Medical Genetics

JF - European Journal of Medical Genetics

SN - 1769-7212

IS - 7

ER -

ID: 138502706