Literature DB >> 6711563

Distal 15q trisomy: phenotypic comparison of nine cases in an extended family.

P Schnatterly, K L Bono, M Robinow, H E Wyandt, N Kardon, T E Kelly.   

Abstract

Nine related individuals have been identified as being trisomic for the distal part of the long arm of chromosome 15 (15q23 to 15qter). The physical characteristics, especially the facial features, of these nine cases are similar and distinctive. These include: facial asymmetry, down-slanting palpebral fissures, ptosis, prominent nose, long philtrum, down-turned mouth, midline crease in the lower lip, puffy cheeks, and micrognathia. By comparing related individuals with the same translocation, the variability due to different breakpoints can be eliminated. Clinical similarities between unrelated individuals with similar duplicated 15q material, but differing second chromosomes, suggest that the phenotype is due to the extra distal 15q chromosomal material. We conclude that distal 15q trisomy produces a clinically recognizable syndrome.

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Year:  1984        PMID: 6711563      PMCID: PMC1684424     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  13 in total

1.  An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.

Authors:  M M Cohen; A Ornoy; A Rosenmann; G Kohn
Journal:  Ann Genet       Date:  1975-06

2.  A G-like trisomy with a major 15 proximal supernumerary component derived from a D/E balanced maternal interchange.

Authors:  D L Bannister; E Engel
Journal:  J Pediatr       Date:  1975-06       Impact factor: 4.406

3.  Letter: Partial trisomy 15 as a result of an unbalanced 12/15 translocation in a patient with a cloverleaf skull anomaly.

Authors:  C Pedersen
Journal:  Clin Genet       Date:  1976-03       Impact factor: 4.438

4.  [Distal trisomy 15q].

Authors:  C Turleau; J de Grouchy; F Chavin-Colin; M Roubin
Journal:  Ann Genet       Date:  1977-09

5.  Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15.

Authors:  R R Schreck; W R Breg; B F Erlanger; O J Miller
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

6.  Inherited partial duplication of chromosome No. 15.

Authors:  A Fujimoto; J W Towner; A J Ebbin; E J Kahlstrom; M G Wilson
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

7.  [Partial trisomy for the distal part of the long arm of chromosome 15 due to a balanced maternal X/15 tranlsocation].

Authors:  B Zabel; W Baumann
Journal:  Ann Genet       Date:  1977-12

8.  Inherited parital duplication deficiency of chromosome 15 (p12;q22).

Authors:  R Coco; V B Penchaszadeh
Journal:  J Genet Hum       Date:  1978-09

9.  Preferential maternal derivation in inv dup(15): analysis of eight new cases.

Authors:  P Maraschio; O Zuffardi; F Bernardi; M Bozzola; C De Paoli; C Fonatsch; S D Flatz; L Ghersini; G Gimelli; M Loi; R Lorini; D Peretti; L Poloni; D Tonetti; R Vanni; G Zamboni
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

10.  Two familial cases with trisomy 15q dist due to a rcp(5;15)(p14;q21).

Authors:  M Tzancheva; M Krachounova; Z Damjanova
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

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  4 in total

1.  Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.

Authors:  D Wieczorek; H Engels; R Viersbach; B Henke; G Schwanitz; E Passarge
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

2.  Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter.

Authors:  Frenny Sheth; Joris Andrieux; Stuti Tewari; Harsh Sheth; Manisha Desai; Pritti Kumari; Nidhish Nanavaty; Jayesh Sheth
Journal:  Mol Cytogenet       Date:  2013-07-01       Impact factor: 2.009

3.  Partial trisomy of chromosome 15q and partial monopsony of 6q due to maternal balanced translocation.

Authors:  Shilpy Singla; Kausik Mandal; Suvasini Sharma; Viswas Chhapola
Journal:  J Pediatr Neurosci       Date:  2014-05

4.  Chromosome 15 structural abnormalities: effect on IGF1R gene expression and function.

Authors:  Rossella Cannarella; Teresa Mattina; Rosita A Condorelli; Laura M Mongioì; Giuseppe Pandini; Sandro La Vignera; Aldo E Calogero
Journal:  Endocr Connect       Date:  2017-10       Impact factor: 3.335

  4 in total

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