Literature DB >> 22855654

Interstitial 4q Deletion and Isodicentric Y-Chromosome in a Patient with Dysmorphic Features.

T I Mancini1, M M Oliveira, A R N Dutra, A B A Perez, R M Minillo, S S Takeno, M I Melaragno.   

Abstract

We present a 2-year-old boy with a de novo 46,XY,idic(Y)(q11.221),del(4)(q26q31.1) karyotype. G-banding, FISH, MLPA, and SNP-array techniques were used to characterize the 24-Mb deletion in 4q and the breakpoint in the isodicentric Y-chromosome region between 15,982,252 and 15,989,842 bp. The patient presented with mild facial dysmorphism, hemangioma, mild frontal cerebral atrophy, and Dandy-Walker variant. Essentially, this case reveals that patients can present more complex genomic imbalances than initially suspected.

Entities:  

Year:  2012        PMID: 22855654      PMCID: PMC3398833          DOI: 10.1159/000338468

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  33 in total

1.  A rare Y chromosome constitutional rearrangement: a partial AZFb deletion and duplication within chromosome Yp in an infertile man with severe oligoasthenoteratozoospermia.

Authors:  Y C Shi; Y X Cui; Y C Zhou; L Wei; H T Jiang; X Y Xia; H Y Lu; H Y Wang; X J Shang; W M Zhu; X J Li; Y F Huang
Journal:  Int J Androl       Date:  2011-10

2.  PAR1 deletions downstream of SHOX are the most frequent defect in a Spanish cohort of Léri-Weill dyschondrosteosis (LWD) probands.

Authors:  Sara Benito-Sanz; Darya Gorbenko del Blanco; Miriam Aza-Carmona; Luis F Magano; Pablo Lapunzina; Jesús Argente; Angel Campos-Barros; Karen E Heath
Journal:  Hum Mutat       Date:  2006-10       Impact factor: 4.878

Review 3.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

4.  High incidence of SHOX anomalies in individuals with short stature.

Authors:  C Huber; M Rosilio; A Munnich; V Cormier-Daire
Journal:  J Med Genet       Date:  2006-04-05       Impact factor: 6.318

5.  Clinical and molecular evaluation of SHOX/PAR1 duplications in Leri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS).

Authors:  S Benito-Sanz; E Barroso; D Heine-Suñer; A Hisado-Oliva; V Romanelli; J Rosell; A Aragones; M Caimari; J Argente; J L Ross; A R Zinn; R Gracia; P Lapunzina; A Campos-Barros; K E Heath
Journal:  J Clin Endocrinol Metab       Date:  2010-12-08       Impact factor: 5.958

6.  An evolutionarily conserved N-terminal acetyltransferase complex associated with neuronal development.

Authors:  Naoaki Sugiura; Suzanne M Adams; Roderick A Corriveau
Journal:  J Biol Chem       Date:  2003-07-29       Impact factor: 5.157

7.  Impaired cerebral cortex development and blood pressure regulation in FGF-2-deficient mice.

Authors:  R Dono; G Texido; R Dussel; H Ehmke; R Zeller
Journal:  EMBO J       Date:  1998-08-03       Impact factor: 11.598

Review 8.  Genomic microarrays in mental retardation: a practical workflow for diagnostic applications.

Authors:  David A Koolen; Rolph Pfundt; Nicole de Leeuw; Jayne Y Hehir-Kwa; Willy M Nillesen; Ineke Neefs; Ine Scheltinga; Erik Sistermans; Dominique Smeets; Han G Brunner; Ad Geurts van Kessel; Joris A Veltman; Bert B A de Vries
Journal:  Hum Mutat       Date:  2009-03       Impact factor: 4.878

9.  Mouse homologues of the human AZF candidate gene RBM are expressed in spermatogonia and spermatids, and map to a Y chromosome deletion interval associated with a high incidence of sperm abnormalities.

Authors:  S K Mahadevaiah; T Odorisio; D J Elliott; A Rattigan; M Szot; S H Laval; L L Washburn; J R McCarrey; B M Cattanach; R Lovell-Badge; P S Burgoyne
Journal:  Hum Mol Genet       Date:  1998-04       Impact factor: 6.150

10.  Mechanisms for human genomic rearrangements.

Authors:  Wenli Gu; Feng Zhang; James R Lupski
Journal:  Pathogenetics       Date:  2008-11-03
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  1 in total

1.  Microarray Analysis of Copy Number Variants on the Human Y Chromosome Reveals Novel and Frequent Duplications Overrepresented in Specific Haplogroups.

Authors:  Martin M Johansson; Anneleen Van Geystelen; Maarten H D Larmuseau; Srdjan Djurovic; Ole A Andreassen; Ingrid Agartz; Elena Jazin
Journal:  PLoS One       Date:  2015-08-31       Impact factor: 3.240

  1 in total

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