Literature DB >> 9507399

MRI findings in a patient with partial monosomy 10p.

F Sunada1, F C Rash, D A Tam.   

Abstract

Partial monosomy 10p is a rare chromosomal disorder characterised by frontal bossing, micrognathia, congenital heart defects, vesicoureteral abnormalities, and developmental delay. This is the first report to describe seizures not associated with hypocalcaemia, as well as cortical atrophy and decreased white matter volume on magnetic resonance imaging, in a patient with documented partial monosomy 10p. The neuroradiographic abnormalities found in this patient provide a first step towards understanding the aetiology of the developmental delay and ventriculomegaly associated with this chromosomal abnormality.

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Year:  1998        PMID: 9507399      PMCID: PMC1051224          DOI: 10.1136/jmg.35.2.159

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


  18 in total

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Review 5.  Family with partial monosomy 10p and trisomy 10p.

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Journal:  Am J Med Genet       Date:  1995-03-27

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Journal:  Eur J Pediatr       Date:  1981-10       Impact factor: 3.183

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Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

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  2 in total

Review 1.  Telomeres: a diagnosis at the end of the chromosomes.

Authors:  B B A De Vries; R Winter; A Schinzel; C van Ravenswaaij-Arts
Journal:  J Med Genet       Date:  2003-06       Impact factor: 6.318

Review 2.  An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14.

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Journal:  J Med Genet       Date:  2000-01       Impact factor: 6.318

  2 in total

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