» Articles » PMID: 1959917

Trisomy 16q23----qter Arising from a Maternal T(13;16)(p12;q23): Case Report and Evidence of the Reciprocal Balanced Maternal Rearrangement by the Ag-NOR Technique

Overview
Journal Hum Genet
Specialty Genetics
Date 1991 Nov 1
PMID 1959917
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

We describe a female new-born with partial trisomy of the long arm of chromosome 16. The chromosome anomaly was the result of an unbalanced segregation of a maternal translocation t(13;16)(p12;q23). Dynamic (RBG, GBG) banding and the Ag-NOR technique ascertained the reciprocal balanced maternal translocation between the 16q23----qter and 13q12----pter segments because nucleolar organizers were present on the tip of long arms of the derivative 16 maternal chromosome. As monosomy 13p has little or no deleterious effect we consider our case as exhibiting the phenotype of trisomy 16q23----qter free from any monosomic feature. Clinical effects are of less consequence as compared with previously published cases of partial trisomy 16q.

Citing Articles

Genetic analysis of partial duplication of the long arm of chromosome 16.

Tang D, Chen A, Xu J, Huang Y, Fan J, Wang J BMC Med Genomics. 2024; 17(1):294.

PMID: 39716170 PMC: 11667835. DOI: 10.1186/s12920-024-02059-3.


A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature.

Manor J, Dinu D, Azamian M, Bi W, Darilek S, Lalani S Am J Med Genet A. 2021; 185(10):2903-2912.

PMID: 34061437 PMC: 9082733. DOI: 10.1002/ajmg.a.62368.


Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.

Mishra R, Paththinige C, Sirisena N, Nanayakkara S, Kariyawasam U, Dissanayake V BMC Pediatr. 2018; 18(1):4.

PMID: 29310616 PMC: 5759277. DOI: 10.1186/s12887-017-0980-z.

References
1.
Howell W, Black D . Controlled silver-staining of nucleolus organizer regions with a protective colloidal developer: a 1-step method. Experientia. 1980; 36(8):1014-5. DOI: 10.1007/BF01953855. View

2.
Lessick M, Israel J, Wong P, Szego K . Partial trisomy 16q secondary to a maternal 9;16 translocation. J Med Genet. 1989; 26(1):63-4. PMC: 1015542. DOI: 10.1136/jmg.26.1.63. View

3.
Garau A, Crisponi G, Peretti D, Vanni R, Zuffardi O . Trisomy 16q21 = to qter. Hum Genet. 1980; 53(2):165-7. DOI: 10.1007/BF00273489. View

4.
Davison E, Beesley J . Partial trisomy 16 as a result of familial 16;20 translocation. J Med Genet. 1984; 21(5):384-6. PMC: 1049325. DOI: 10.1136/jmg.21.5.384. View

5.
NEU R, Ortega C, Barg G, Pinto Jr W, GARDNER L, Howell W . Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18. J Med Genet. 1976; 13(6):520-2. PMC: 1013484. DOI: 10.1136/jmg.13.6.520. View