Literature DB >> 9375722

Inherited inverted duplication of X chromosome in a male: report of a patient and review of the literature.

M Shapira1, H Dar, H Bar-El, N Bar-Nitzan, L Even, Z Borochowitz.   

Abstract

Nineteen cases of duplication of segments of the long arm of chromosome X have been published in 13 males and in 6 females. We report an additional case of a male with growth and mental retardation, growth hormone deficiency, compensated primary hypothyroidism, distinctive anomalies of the face, hypoplastic genitalia, and hypotonia in whom inverted duplication of a segment in the long arm of X chromosome was diagnosed, 46,Y, dup (X)(q21.2q13.3), and mosaicism was demonstrated in his mother's X chromosome. The rearranged segment was diagnosed utilizing high resolution G-band technique and FISH studies, using chromosome X total chromosome probe and DNA XIST probe. This appears to be the first report of a patient with duplication of Xq and hypothyroidism.

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Year:  1997        PMID: 9375722     DOI: 10.1002/(sici)1096-8628(19971112)72:4<409::aid-ajmg7>3.0.co;2-l

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


  7 in total

1.  Xq21.1q21.31 Duplication in Two Male Siblings.

Authors:  Charlotte Ann Sherlaw-Sturrock; Sarah Graham; Anita Morgan; Lisa Reali; Swati Naik
Journal:  Mol Syndromol       Date:  2021-11-01

2.  Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition.

Authors:  Marlène Rio; Valérie Malan; Sarah Boissel; Annick Toutain; Ghislaine Royer; Stéphanie Gobin; Nicole Morichon-Delvallez; Catherine Turleau; Jean-Paul Bonnefont; Arnold Munnich; Michel Vekemans; Laurence Colleaux
Journal:  Eur J Hum Genet       Date:  2009-10-21       Impact factor: 4.246

3.  Subterminal deletion/duplication event in an affected male due to maternal X chromosome pericentric inversion.

Authors:  Nadja Kokalj-Vokac; Natasa Marcun-Varda; Andreja Zagorac; Alenka Erjavec-Skerget; Boris Zagradisnik; Mirjana Todorovic; Alojz Gregoric
Journal:  Eur J Pediatr       Date:  2004-08-12       Impact factor: 3.183

4.  A case report of two male siblings with autism and duplication of Xq13-q21, a region including three genes predisposing for autism.

Authors:  Elisabet Wentz; Mihailo Vujic; Ewa-Lotta Kärrstedt; Anna Erlandsson; Christopher Gillberg
Journal:  Eur Child Adolesc Psychiatry       Date:  2013-08-23       Impact factor: 4.785

5.  A novel de novo partial xq duplication in a girl with short stature, nonverbal learning disability and diminished ovarian reserve - effect of growth hormone treatment and fertility preservation strategies: a case report and up-to-date review.

Authors:  Francesca Parissone; Mairi Pucci; Emanuela Meneghelli; Orsetta Zuffardi; Rossana Di Paola; Stefano Zaffagnini; Massimo Franchi; Elisabetta Santangelo; Gaetano Cantalupo; Paolo Cavarzere; Franco Antoniazzi; Giorgio Piacentini; Rossella Gaudino
Journal:  Int J Pediatr Endocrinol       Date:  2020-01-09

6.  A 5.8 Mb interstitial deletion on chromosome Xq21.1 in a boy with intellectual disability, cleft palate, hearing impairment and combined growth hormone deficiency.

Authors:  M Giordano; C Gertosio; S Pagani; C Meazza; I Fusco; E Bozzola; M Bozzola
Journal:  BMC Med Genet       Date:  2015-09-01       Impact factor: 2.103

7.  Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterization.

Authors:  Natália D Linhares; Eugênia R Valadares; Silvia S da Costa; Rodrigo R Arantes; Luiz Roberto de Oliveira; Carla Rosenberg; Angela M Vianna-Morgante; Marta Svartman
Journal:  Meta Gene       Date:  2016-07-07
  7 in total

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