Literature DB >> 8362903

Case of ring chromosome 7: the first report of neuropathological findings.

H Tsukamoto1, N Sakai, M Taniike, M Nakatsukasa, W Yoshiwara, H Sakamoto, H Fujimura, K Inui, S Okada.   

Abstract

We report on a boy with ring chromosome 7 who had severe mental retardation, growth failure, microcephaly, cleft lip and palate, café-au-lait spots, nevus flammeus, and genital abnormalities, and died of pneumonia at age 20 months. On autopsy he had fusion of the anterior cerebral hemispheres, accompanied by agenesis of olfactory bulbs and tracts, closely resembling those found in semilobar holoprosencephaly. In addition, heterotopic Purkinje cell clusters in the cerebellar white matter, absence of pigmentation within the brainstem pigmented neurons, and severe hypomyelination in the whole brain were noted. The patient may represent the most severe manifestation of ring chromosome 7, and this is the first detailed neuropathological report on this subject.

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Year:  1993        PMID: 8362903     DOI: 10.1002/ajmg.1320460606

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  Cytogenetic findings indicate heterogeneity in patients with blepharophimosis, epicanthus inversus, and developmental delay.

Authors:  M Warburg; M Bugge; K Brøndum-Nielsen
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

2.  Molecular cytogenetic analysis and clinical manifestations of a case with de novo mosaic ring chromosome 7.

Authors:  Li-Ping Tsai; Kuei-Fang Lee; Jye-Siung Fang; Ingrid Y Liu
Journal:  Mol Cytogenet       Date:  2011-02-08       Impact factor: 2.009

3.  First trimester diagnosis of holoprosencephaly secondary to a ring chromosome 7.

Authors:  Lindsay B Henderson; Virginia L Corson; Daniel O Saul; Cynthia Anderson; Sarah Millard; Denise A S Batista; Karin J Blakemore; Cheryl Descipio
Journal:  Case Rep Genet       Date:  2013-02-21
  3 in total

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