Literature DB >> 7584707

Familial blepharophimosis: an uncommon marker of ovarian dysgenesis.

M Nicolino1, M Bost, M David, J L Chaussain.   

Abstract

We report on six young female patients from two families who were found to have a very rare form of ovarian failure. Hypogonadism is inherited with an ocular abnormality consisting of a congenital dysplasia of the eyelids. In one family inheritance is autosomal dominant and in the other it is a de novo mutation. The patients have no other dysmorphic features and are of normal intelligence. Plasma levels of follicle-stimulating and luteinizing hormones are significantly elevated. Examination of the internal genitalia by laparoscopy was performed in four cases with ovarian biopsy in one case; the results are compatible with gonadal dysgenesis. Cytogenetic studies indicate the absence of chromosomal defects.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7584707     DOI: 10.1515/jpem.1995.8.2.127

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  3 in total

Review 1.  A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q.

Authors:  T Cai; D A Tagle; X Xia; P Yu; X X He; L Y Li; J H Xia
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

2.  A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23.

Authors:  P Amati; P Gasparini; J Zlotogora; L Zelante; J C Chomel; A Kitzis; J Kaplan; D Bonneau
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

3.  The forkhead transcription factor FOXL2 is expressed in somatic cells of the human ovary prior to follicle formation.

Authors:  K Duffin; R A L Bayne; A J Childs; C Collins; R A Anderson
Journal:  Mol Hum Reprod       Date:  2009-08-25       Impact factor: 4.025

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.