Literature DB >> 11241465

Interstitial deletion 4q32-34 with ulnar deficiency: 4q33 may be the critical region in 4q terminal deletion syndrome.

S L Keeling1, L Lee-Jones, P Thompson.   

Abstract

We report on an infant with Robin sequence; mild developmental delay; a left ulnar ray defect with absent ulna and associated metacarpals, carpals and phalanges; and a right ulnar nerve hypoplasia. He had a de novo interstitial deletion of 4q32-->q34. The critical region involved in the 4q terminal deletion syndrome may be 4q33. This conclusion was suggested by showing that del(4)(q31qter), del(4)(q32qter), and del(4)(q33qter) result in a similarly severe phenotype. In addition, we propose that genes for distal arm development, in particular for development of the left ulnar ray, central nervous system development, and cleft lip and palate, may be located at 4q33. Copyright 2001 Wiley-Liss, Inc.

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Mesh:

Year:  2001        PMID: 11241465     DOI: 10.1002/1096-8628(2000)9999:999<00::aid-ajmg1134>3.0.co;2-d

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


  10 in total

1.  4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome.

Authors:  Goran Cuturilo; Björn Menten; Aleksandar Krstic; Danijela Drakulic; Ida Jovanovic; Vojislav Parezanovic; Milena Stevanovic
Journal:  Eur J Pediatr       Date:  2011-07-22       Impact factor: 3.183

2.  Hand2 function in second heart field progenitors is essential for cardiogenesis.

Authors:  Takatoshi Tsuchihashi; Jun Maeda; Chong H Shin; Kathryn N Ivey; Brian L Black; Eric N Olson; Hiroyuki Yamagishi; Deepak Srivastava
Journal:  Dev Biol       Date:  2010-12-23       Impact factor: 3.582

3.  Analysis of genetic characteristics of 436 children with dysplasia and detailed analysis of rare karyotype.

Authors:  Zong-Yu Miao; Shi-Feng Chen; Hong Wu; Xiao-Yan Liu; Hui-Yuan Shao
Journal:  Open Life Sci       Date:  2022-04-26       Impact factor: 1.311

Review 4.  Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature.

Authors:  Michael R Rossi; Miriam S DiMaio; Bixia Xiang; Kangmo Lu; Hande Kaymakcalan; Margretta Seashore; Maurice J Mahoney; Peining Li
Journal:  Am J Med Genet A       Date:  2009-12       Impact factor: 2.802

5.  Renal failure associated with APECED and terminal 4q deletion: evidence of autoimmune nephropathy.

Authors:  Mohammed Al-Owain; Namik Kaya; Hamad Al-Zaidan; Ibrahim Bin Hussain; Hadeel Al-Manea; Hindi Al-Hindi; Shelley Kennedy; M Anwar Iqbal; Hamad Al-Mojalli; Albandary Al-Bakheet; Anne Puel; Jean-Laurent Casanova; Saleh Al-Muhsen
Journal:  Clin Dev Immunol       Date:  2010-12-14

6.  Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.

Authors:  Karine Morcel; Tanguy Watrin; Laurent Pasquier; Lucie Rochard; Cédric Le Caignec; Christèle Dubourg; Philippe Loget; Bernard-Jean Paniel; Sylvie Odent; Véronique David; Isabelle Pellerin; Claude Bendavid; Daniel Guerrier
Journal:  Orphanet J Rare Dis       Date:  2011-03-15       Impact factor: 4.123

7.  Novel copy number variants in children with autism and additional developmental anomalies.

Authors:  L K Davis; K J Meyer; D S Rudd; A L Librant; E A Epping; V C Sheffield; T H Wassink
Journal:  J Neurodev Disord       Date:  2009-05-27       Impact factor: 4.025

8.  Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans.

Authors:  Amira Elmakky; Ilaria Stanghellini; Antonio Landi; Antonio Percesepe
Journal:  Curr Genomics       Date:  2015-08       Impact factor: 2.236

Review 9.  Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.

Authors:  Barbara Vona; Indrajit Nanda; Cordula Neuner; Jörg Schröder; Vera M Kalscheuer; Wafaa Shehata-Dieler; Thomas Haaf
Journal:  BMC Med Genet       Date:  2014-06-25       Impact factor: 2.103

10.  Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array.

Authors:  Pingping Zhang; Yanmei Sun; Ping Huo; Haishen Tian; Jian Gao; Yali Li
Journal:  Mol Cytogenet       Date:  2020-04-10       Impact factor: 2.009

  10 in total

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