Literature DB >> 1153226

The ovarian dysgenesis of trisomy 18.

P Russell, G Altshuler.   

Abstract

Ovarian abnormalities have been reported as a rare feature of the trisomy 18 syndrome. Gross and histological examination of autopsy material from 13 female infants with this syndrome revealed that ovarian dysgenesis, in varying degrees of severity, is more common than is indicated by the literature. The characteristic changes are reduction in germ cells due to necrobiosis, and the presence of mesothelial clefts and abnormal masses of stromal cells.

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Year:  1975        PMID: 1153226     DOI: 10.3109/00313027509092711

Source DB:  PubMed          Journal:  Pathology        ISSN: 0031-3025            Impact factor:   5.306


  4 in total

Review 1.  The genetics of human reproduction.

Authors:  A C Chandley
Journal:  Experientia       Date:  1986-10-15

2.  Prophase pairing in a mosaic 18p-;iso 18q human female foetus studied by surface spreading.

Authors:  R M Speed
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

3.  Ovarian dysgenesis in individuals with chromosomal abnormalities.

Authors:  C Cunniff; K L Jones; K Benirschke
Journal:  Hum Genet       Date:  1991-04       Impact factor: 4.132

4.  Balanced autosomal translocations and ovarian dysgenesis.

Authors:  R Tupler; L Barbierato; D Larizza; P Sampaolo; F Piovella; P Maraschio
Journal:  Hum Genet       Date:  1994-08       Impact factor: 4.132

  4 in total

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