| Literature DB >> 8362903 |
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.Entities:
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Year: 1993 PMID: 8362903 DOI: 10.1002/ajmg.1320460606
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299