YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome

Marga Nadal, Montserrat Milà, Melanie Pritchard, Antonio Mur, Josep Pujals, Jean Louis Blouin, Stylianos E. Antonarakis, Francesca Ballesta, Xavier P. Estivill

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Most cases of Down syndrome (DS) result from a supernumerary chromosome 21; however, there are rare cases in which DS is due to partial trisomy of chromosome 21, involving various segments of the chromosome. The characterization of cases of DS that are due to partial trisomy 21 allows the phenotype to be correlated with the genotype. We present a case with features of DS and a partial trisomy of chromosome 21 inherited from a paternal balanced translocation involving chromosomes 13 and 21. Fluorescence in situ hybridization analysis using yeast artificial chromosome (YAC) probes mapped the breakpoint to 21q22.1, within YAC 230E8, which contains markers CBR, D21S333 and D21S334. Further mapping using cosmid positioned the breakpoint proximal to CBR. The patient was also monosomic for the distal portion of chromosome 13 (q33-qter). Many phenotypic features of DS were present including hypotonia, flat occiput, flat facies, up-slanted palpebral fissures, epicanthic folds, flat nasal bridge, macroglossia, open mouth, small ears and a heart murmur. This case further supports the contention that the majority of the phenotypic features of DS map to 21q22-qter and further refines the location of some of them. In addition to the DS phenotype, the patient had a prominent upper maxilla with protruding upper incisors, and low levels of the coagulation factors VII and X, consistent with a syndrome resulting from monosomy 13q33-qter. Since some features overlap between the two syndromes, including severe mental retardation, it is unclear to what extent monosmy for 13q33-qter, trisomy for 21q22.1-qter, or a combination of both, contributed to the common features of the phenotype.

Original languageEnglish
Pages (from-to)460-466
Number of pages7
JournalHuman Genetics
Volume98
Issue number4
DOIs
Publication statusPublished - 1996
Externally publishedYes

Fingerprint

Yeast Artificial Chromosomes
Cosmids
Genetic Translocation
Down Syndrome
Chromosomes, Human, Pair 21
Trisomy
Chromosomes, Human, Pair 13
Phenotype
Macroglossia
Heart Murmurs
Monosomy
Factor X
Factor VII
Muscle Hypotonia
Maxilla
Eyelids
Incisor
Fluorescence In Situ Hybridization
Nose
Intellectual Disability

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome. / Nadal, Marga; Milà, Montserrat; Pritchard, Melanie; Mur, Antonio; Pujals, Josep; Blouin, Jean Louis; Antonarakis, Stylianos E.; Ballesta, Francesca; Estivill, Xavier P.

In: Human Genetics, Vol. 98, No. 4, 1996, p. 460-466.

Research output: Contribution to journalArticle

Nadal, M, Milà, M, Pritchard, M, Mur, A, Pujals, J, Blouin, JL, Antonarakis, SE, Ballesta, F & Estivill, XP 1996, 'YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome', Human Genetics, vol. 98, no. 4, pp. 460-466. https://doi.org/10.1007/s004390050240
Nadal, Marga ; Milà, Montserrat ; Pritchard, Melanie ; Mur, Antonio ; Pujals, Josep ; Blouin, Jean Louis ; Antonarakis, Stylianos E. ; Ballesta, Francesca ; Estivill, Xavier P. / YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome. In: Human Genetics. 1996 ; Vol. 98, No. 4. pp. 460-466.
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AU - Milà, Montserrat

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AU - Mur, Antonio

AU - Pujals, Josep

AU - Blouin, Jean Louis

AU - Antonarakis, Stylianos E.

AU - Ballesta, Francesca

AU - Estivill, Xavier P.

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