Literature DB >> 8357009

Isochromosome 18p in a mother and her child.

D Abeliovich1, J Dagan, A Levy, A Steinberg, J Zlotogora.   

Abstract

We present a familial case of isochromosome 18p [i(18p)] as a supernumerary chromosome. The mother, who is a mosaic for i(18p) with partial tetrasomy 18p syndrome, transmitted the isochromosome to her only child. The child has the full syndrome of tetrasomy 18p. This is the first case of mosaicism i(18p) in an adult patient with clinical manifestations.

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Year:  1993        PMID: 8357009     DOI: 10.1002/ajmg.1320460409

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


  14 in total

1.  De novo isochromosome 18p in a female dysmorphic child.

Authors:  Smitha Ramegowda; Harshavardhan M Gawde; Abbas Hyderi; Mysore R Savitha; Zareen M Patel; Balasundaram Krishnamurthy; Nallur B Ramachandra
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

2.  Tetrasomy 18p in a male dysmorphic child in southeast Turkey.

Authors:  Mahmut Balkan; Hatun Duran; Turgay Budak
Journal:  J Genet       Date:  2009-12       Impact factor: 1.166

3.  Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniques.

Authors:  M B Qumsiyeh; A Tomasi; M Taslimi
Journal:  J Med Genet       Date:  1995-12       Impact factor: 6.318

4.  Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing.

Authors:  T Eggermann; H Engels; B Moskalonek; M M Nöthen; J Müller-Navia; E Schleiermacher; G Schwanitz; S Stengel-Rutkowski
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

5.  Update and Review: Supernumerary Marker Chromosomes.

Authors:  S Ungerleider
Journal:  J Genet Couns       Date:  2000-08       Impact factor: 2.537

6.  [Tetrasomy 18p syndrome and hearing loss. An unusual case].

Authors:  C Schwemmle; M Arslan-Kirchner; B Pabst; M Ptok
Journal:  HNO       Date:  2012-10       Impact factor: 1.284

7.  A rare chromosomal disorder - isochromosome 18p syndrome.

Authors:  Vasilica Plaiasu; Diana Ochiana; Gabriela Motei; Adrian Georgescu
Journal:  Maedica (Buchar)       Date:  2011-04

8.  Adults with Chromosome 18 Abnormalities.

Authors:  Bridgette Soileau; Minire Hasi; Courtney Sebold; Annice Hill; Louise O'Donnell; Daniel E Hale; Jannine D Cody
Journal:  J Genet Couns       Date:  2014-11-19       Impact factor: 2.537

9.  A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report.

Authors:  Hela Bellil; Bérenice Herve; Elodie Herzog; Jean-Marc Ayoubi; François Vialard; Marine Poulain
Journal:  J Assist Reprod Genet       Date:  2020-01-24       Impact factor: 3.412

Review 10.  Small supernumerary marker chromosomes and their correlation with specific syndromes.

Authors:  Hamideh Jafari-Ghahfarokhi; Maryam Moradi-Chaleshtori; Thomas Liehr; Morteza Hashemzadeh-Chaleshtori; Hossein Teimori; Payam Ghasemi-Dehkordi
Journal:  Adv Biomed Res       Date:  2015-07-27
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