Literature DB >> 3791676

Klinefelter's syndrome in Sardinia. Clinical report of 265 hypogonadic males detected at the time of military check-up.

G Filippi.   

Abstract

265 hypogonadic Sardinian males, ascertained through military records of 600,000 conscripts approximately over the last thirty-seven years, were screened for their sex chromatin phenotype by buccal mucosa smears and for their karyotypes from peripheral blood lymphocyte cultures. 158 (59.4%) showed a XXY karyotype without mosaicism, 5 XX and 1 XXYY karyotypes. Seven sex chromatin negative males had Kallmann's syndrome. This report summarizes the genetic and clinical data recorded in this population sample as opposed to those reported from fertility clinics.

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Year:  1986        PMID: 3791676

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  7 in total

1.  Klinefelter's syndrome in Sardinia and Scotland. Comparative studies of parental age and other aetiological factors in 47,XXY.

Authors:  A D Carothers; G Filippi
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

2.  Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

3.  Mice harboring Gnrhr E90K, a mutation that causes protein misfolding and hypogonadotropic hypogonadism in humans, exhibit testis size reduction and ovulation failure.

Authors:  M David Stewart; Jian Ming Deng; C Allison Stewart; Rachael D Mullen; Ying Wang; Suhujey Lopez; M Katalina Serna; Cheng-Chiu Huang; Jo Ann Janovick; Andrew J Pask; Robert J Schwartz; P Michael Conn; Richard R Behringer
Journal:  Mol Endocrinol       Date:  2012-08-23

4.  Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland.

Authors:  Eeva-Maria Laitinen; Kirsi Vaaralahti; Johanna Tommiska; Elina Eklund; Mari Tervaniemi; Leena Valanne; Taneli Raivio
Journal:  Orphanet J Rare Dis       Date:  2011-06-17       Impact factor: 4.123

5.  Clinical and inheritance profiles of Kallmann syndrome in Jordan.

Authors:  Mousa A Abujbara; Hanan A Hamamy; Nadim S Jarrah; Nadima S Shegem; Kamel M Ajlouni
Journal:  Reprod Health       Date:  2004-10-24       Impact factor: 3.223

6.  Recombinant Human FSH Treatment Outcomes in Five Boys With Severe Congenital Hypogonadotropic Hypogonadism.

Authors:  Ella Kohva; Hanna Huopio; Matti Hero; Päivi J Miettinen; Kirsi Vaaralahti; Virpi Sidoroff; Jorma Toppari; Taneli Raivio
Journal:  J Endocr Soc       Date:  2018-10-15

7.  A Family With Novel X-Linked Recessive Homozygous Mutation in ANOS1 (c.628_629 del, p.1210fs∗) in Kallmann Syndrome Associated Unilateral Ptosis: Case Report and Literature Review.

Authors:  Shahab Noorian; Shahram Savad; Armin Khavandegar; Mahnaz Jamee
Journal:  AACE Clin Case Rep       Date:  2021-02-17
  7 in total

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