Literature DB >> 604495

Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.

A Schinzel, P Auf der Maur, H Moser.   

Abstract

Two cases, a boy and a girl, with the 11q-(Jacobsen) syndrome are reported. Findings common to both and typical for this chromosome aberration include a narrow protruding forehead, hypertelorism, non-horizontal position of the eyes, ptosis, strabismus, broad root, and short upturned tip of thenose, carp mouth, receding chin, misshapen ears, simian creases, and severe mental retardation. In addition, one patient had pyloric stenosis and an inguinal hernia. Growth retardation and microcephaly were not found in either of them. The karyotypes revealed de novo-deletions of the long arm of one chromosome 11,del(11)(q23).

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Year:  1977        PMID: 604495      PMCID: PMC1013641          DOI: 10.1136/jmg.14.6.438

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  21 in total

1.  Chromosome 11 long arm partial deletion: a new syndrome.

Authors:  E Engel; C S Hirshberg; S B Cassidy; B J McGee
Journal:  Am J Ment Defic       Date:  1976-01

2.  The 11q-- syndrome: another case report.

Authors:  M T Mulcahy; J Jenkyn
Journal:  Hum Genet       Date:  1977-04-15       Impact factor: 4.132

3.  [Partial monosomy 11q. A new case].

Authors:  J L Bresson; A Noir
Journal:  Ann Genet       Date:  1977-03

4.  Trigonocephaly and the 11q- syndrome.

Authors:  S B Cassidy; R M Heller; A W Kilroy; W McKelvey; E Engel
Journal:  Ann Genet       Date:  1977-03

5.  [Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine].

Authors:  B Dutrillaux; C Laurent; J Couturier; J Lejeune
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1973-06-13

6.  A rapid banding technique for routine use in human and comparative cytogenetics.

Authors:  K Sperling; R Wiesner
Journal:  Humangenetik       Date:  1972

7.  The 11q -- syndrome.

Authors:  J Frank; V M Riccardi
Journal:  Hum Genet       Date:  1977-02-11       Impact factor: 4.132

8.  Proximal 4p-deletion: phenotype differs from classical 4p-syndrome.

Authors:  U Francke; D E Arias; W L Nyham
Journal:  J Pediatr       Date:  1977-02       Impact factor: 4.406

9.  Evidence for localisation of genes for human alpha-globin on the long arm of chromosome 4.

Authors:  E Gandini; B Dallapiccola; C Laurent; E F Suerinc; A Forabosco; F Conconi; L Del Senno
Journal:  Nature       Date:  1977-01-06       Impact factor: 49.962

10.  A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9.

Authors:  B Zabel; S Hansen; U Hilig; H Gröting-Imhof
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

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  10 in total

1.  Congenital ocular and other systemic abnormalities associated with ring-11 chromosome.

Authors:  S Daniele; F Pecorelli; L Tiepolo; R Armellini; F S Liotti
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1986       Impact factor: 3.117

2.  Partial deletion of the long arm chromosome 11 in Jacobsen syndrome.

Authors:  K S Reddy; I M Thomas; H S Narayanan
Journal:  Indian J Pediatr       Date:  1986 Jan-Feb       Impact factor: 1.967

3.  Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23.

Authors:  L E Voullaire; G C Webb; M A Leversha
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

Review 4.  Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

Authors:  E K Pivnick; G V Velagaleti; R S Wilroy; M E Smith; S R Rose; R E Tipton; A T Tharapel
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

5.  Partial deletion of the long arm of chromosome 11 the Jacobsen syndrome.

Authors:  K S Reddy; I M Thomas; H S Narayanan
Journal:  Indian J Pediatr       Date:  1984 May-Jun       Impact factor: 1.967

Review 6.  Molecular detection of a translocation (Y;11) (q11.2;q24) in a 45,X male with signs of Jacobsen syndrome.

Authors:  J O Van Hemel; B Eussen; E Wesby-van Swaay; B A Oostra
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

7.  Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition.

Authors:  H Varley; S Di; S W Scherer; N J Royle
Journal:  Am J Hum Genet       Date:  2000-08-01       Impact factor: 11.025

8.  Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype.

Authors:  B M Lippe; R S Sparkes; B Fass; L Neidengard
Journal:  J Med Genet       Date:  1980-12       Impact factor: 6.318

Review 9.  Jacobsen syndrome.

Authors:  Teresa Mattina; Concetta Simona Perrotta; Paul Grossfeld
Journal:  Orphanet J Rare Dis       Date:  2009-03-07       Impact factor: 4.123

10.  Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).

Authors:  Emmanouil Manolakos; Sandro Orru; Rosita Neroutsou; Konstantinos Kefalas; Eirini Louizou; Ioannis Papoulidis; Loretta Thomaidis; Panagiotis Peitsidis; Sotirios Sotiriou; George Kitsos; Panagiota Tsoplou; Michael B Petersen; Aikaterini Metaxotou
Journal:  Mol Cytogenet       Date:  2009-12-09       Impact factor: 2.009

  10 in total

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