Literature DB >> 1734299

Olfactory dysgenesis or hypoplasia: a variant in the arhinencephaly spectrum?

D N Louis1, P V Arriagada, B T Hyman, E T Hedley-Whyte.   

Abstract

Postmortem examination of a 65-year-old anosmic woman revealed rudimentary olfactory bulbs, an imperforate cribriform plate, and sulcal abnormalities of the orbitofrontal surface of the brain. The remainder of the brain, skull, and body was normal. This abnormality most likely resulted from a local insult to the area of the cribriform plate during early fetal life, occurring after the induction of olfactory bulb differentiation, but before migration and complete differentiation of the olfactory bulbs. Such a lesion can be dated to approximately 11 to 12 weeks gestational age. The malformation may represent another variant in the arhinencephaly spectrum, but is termed "olfactory dysgenesis" or "olfactory hypoplasia" to separate it from true olfactory aplasia and arhinencephaly.

Entities:  

Mesh:

Year:  1992        PMID: 1734299     DOI: 10.1212/wnl.42.1.179

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  1 in total

1.  Incidental olfactory aplasia: a case report.

Authors:  K E Dundas; R M Anderson
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-02       Impact factor: 10.154

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.