Literature DB >> 10995509

Hypogonadism and CHARGE association.

P G Wheeler1, C A Quigley, A Sadeghi-Nejad, D D Weaver.   

Abstract

The G of the CHARGE association represents genital hypoplasia, which is typically recognized only in males (micropenis/cryptorchidism). The cause of genital hypoplasia in this disorder has not been determined. We now report the cases of nine individuals with CHARGE association and hypogonadotropic hypogonadism, manifested by hypogenitalism and gonadotropins at or below minimal detectable levels at ages when these hormones should be readily measurable. We suggest that central hypogonadism is responsible not only for the genital hypoplasia in male patients but also for the lack of secondary sexual development in patients of both sexes. Since hypogonadotropic hypogonadism appears to be the usual cause of genital and pubertal abnormalities in CHARGE association, measurement of serum luteinizing hormone (LH) and follicle-stimulating hormone (FSH) concentrations in infants up to 2-3 months of age who are suspected of having this disorder could help establish the diagnosis. Determination of serum LH and FSH concentrations in teenagers with CHARGE association could result in early diagnosis of hypogonadotropic hypogonadism, allowing for treatment of hormonal deficiencies and minimization of potential secondary psychosocial and medical problems. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10995509     DOI: 10.1002/1096-8628(20000918)94:3<228::aid-ajmg8>3.0.co;2-h

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

Review 1.  The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Authors:  Hyung-Goo Kim; Lawrence C Layman
Journal:  Mol Cell Endocrinol       Date:  2011-08-02       Impact factor: 4.102

2.  Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.

Authors:  Ravikumar Balasubramanian; Jin-Ho Choi; Ludmila Francescatto; Jason Willer; Edward R Horton; Eleni P Asimacopoulos; Konstantina M Stankovic; Lacey Plummer; Cassandra L Buck; Richard Quinton; Todd D Nebesio; Veronica Mericq; Paulina M Merino; Brian F Meyer; Dorota Monies; James F Gusella; Nada Al Tassan; Nicholas Katsanis; William F Crowley
Journal:  Proc Natl Acad Sci U S A       Date:  2014-12-03       Impact factor: 11.205

Review 3.  Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

Authors:  Ravikumar Balasubramanian; William F Crowley
Journal:  Am J Med Genet C Semin Med Genet       Date:  2017-11-20       Impact factor: 3.908

4.  Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Authors:  Hyung-Goo Kim; Ingo Kurth; Fei Lan; Irene Meliciani; Wolfgang Wenzel; Soo Hyun Eom; Gil Bu Kang; Georg Rosenberger; Mustafa Tekin; Metin Ozata; David P Bick; Richard J Sherins; Steven L Walker; Yang Shi; James F Gusella; Lawrence C Layman
Journal:  Am J Hum Genet       Date:  2008-10-02       Impact factor: 11.025

5.  Endocrinological Characteristics of 25 Japanese Patients with CHARGE Syndrome.

Authors:  Yasuko Shoji; Shinobu Ida; Yuri Etani; Hiroyuki Yamada; Futoshi Kayatani; Yasuhiro Suzuki; Kenjiro Kosaki; Nobuhiko Okamoto
Journal:  Clin Pediatr Endocrinol       Date:  2014-04-22

Review 6.  Guidelines in CHARGE syndrome and the missing link: Cranial imaging.

Authors:  Christa M de Geus; Rolien H Free; Berit M Verbist; Deborah A Sival; Kim D Blake; Linda C Meiners; Conny M A van Ravenswaaij-Arts
Journal:  Am J Med Genet C Semin Med Genet       Date:  2017-11-23       Impact factor: 3.908

7.  A case of combined 21-hydroxylase deficiency and CHARGE syndrome featuring micropenis and cryptorchidism.

Authors:  Satoko Umino; Miyuki Kitamura; Yuko Katoh-Fukui; Maki Fukami; Takeshi Usui; Shuichi Yatsuga; Yasutoshi Koga
Journal:  Mol Genet Genomic Med       Date:  2019-05-06       Impact factor: 2.183

8.  Effect of long-term GH treatment in a patient with CHARGE association.

Authors:  Andrea Esposito; Maria Tufano; Iolanda Di Donato; Martina Rezzuto; Nicola Improda; Daniela Melis; Mariacarolina Salerno
Journal:  Ital J Pediatr       Date:  2014-06-02       Impact factor: 2.638

  8 in total

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