Literature DB >> 2325096

Identical twins discordant for Kallmann's syndrome.

L J Hipkin1, I F Casson, J C Davis.   

Abstract

A 20 year old male patient presented with lack of sexual development. On examination he was eunuchoidal and hypogonadal, and olfactory function testing showed he was anosmic. Biochemical investigations proved he was hypogonadotrophic. Kallmann's syndrome was therefore diagnosed. His appearance was very different from his alleged identical twin who had undergone a normal puberty and had normal plasma testosterone and gonadotrophin levels. However, the twin was hyposmic. Genetic fingerprinting confirmed the twins were identical. Why Kallman's syndrome was incompletely expressed in one of them is unexplained. The parents and a normally menstruating sister had normal olfactory function.

Entities:  

Mesh:

Year:  1990        PMID: 2325096      PMCID: PMC1017005          DOI: 10.1136/jmg.27.3.198

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  [Parkinson's disease and anosmia in monozygotic twin sisters (author's transl)].

Authors:  P Kissel; J M Andre
Journal:  J Genet Hum       Date:  1976-06

2.  Hypogonadotropic eunuchoidism. I. Clinical study of the mode of inheritance.

Authors:  R J Santen; C A Paulsen
Journal:  J Clin Endocrinol Metab       Date:  1973-01       Impact factor: 5.958

3.  Hypogonadotropic hypogonadism associated with retinitis pigmentosa in a female sibship: evidence for gonadotropin deficiency.

Authors:  R J Chang; B J Davidson; H E Carlson; J K Lu; H L Judd
Journal:  J Clin Endocrinol Metab       Date:  1981-12       Impact factor: 5.958

4.  Heterogeneity of Kallmann's syndrome.

Authors:  M Hermanussen; W G Sippell
Journal:  Clin Genet       Date:  1985-08       Impact factor: 4.438

5.  [Monozygotic twins with schizoform psychosis and hypothalamic-induced hypogonadotropic hypogonadism].

Authors:  A Genz; C Lö SS ner; E Krüger
Journal:  Psychiatr Neurol Med Psychol (Leipz)       Date:  1987-04
  5 in total
  8 in total

1.  Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type.

Authors:  A A Bergen; C Samanns; E J Schuurman; L van Osch; D B van Dorp; A J Pinckers; E Bakker; A Gal; G J van Ommen; E M Bleeker-Wagemakers
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

Review 2.  Isolated GnRH deficiency: a disease model serving as a unique prism into the systems biology of the GnRH neuronal network.

Authors:  Ravikumar Balasubramanian; William F Crowley
Journal:  Mol Cell Endocrinol       Date:  2011-07-12       Impact factor: 4.102

3.  Comments on discordant monozygotic twinning in homosexuality.

Authors:  W J Turner
Journal:  Arch Sex Behav       Date:  1994-02

4.  Next-generation sequencing of patients with congenital anosmia.

Authors:  Anna Alkelai; Tsviya Olender; Catherine Dode; Sagit Shushan; Pavel Tatarskyy; Edna Furman-Haran; Valery Boyko; Ruth Gross-Isseroff; Matthew Halvorsen; Lior Greenbaum; Roni Milgrom; Kazuya Yamada; Ayumi Haneishi; Ilan Blau; Doron Lancet
Journal:  Eur J Hum Genet       Date:  2017-11-13       Impact factor: 4.246

5.  Kallmann syndrome.

Authors:  Catherine Dodé; Jean-Pierre Hardelin
Journal:  Eur J Hum Genet       Date:  2008-11-05       Impact factor: 4.246

6.  Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism.

Authors:  Taneli Raivio; Yisrael Sidis; Lacey Plummer; Huaibin Chen; Jinghong Ma; Abir Mukherjee; Elka Jacobson-Dickman; Richard Quinton; Guy Van Vliet; Helene Lavoie; Virginia A Hughes; Andrew Dwyer; Frances J Hayes; Shuyun Xu; Susan Sparks; Ursula B Kaiser; Moosa Mohammadi; Nelly Pitteloud
Journal:  J Clin Endocrinol Metab       Date:  2009-10-09       Impact factor: 5.958

Review 7.  Kallmann syndrome: fibroblast growth factor signaling insufficiency?

Authors:  Catherine Dodé; Jean-Pierre Hardelin
Journal:  J Mol Med (Berl)       Date:  2004-09-08       Impact factor: 4.599

8.  Invertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.

Authors:  Elia Di Schiavi; Davide Andrenacci
Journal:  Curr Genomics       Date:  2013-03       Impact factor: 2.236

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.