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J Pediatr Genet 2024; 13(02): 106-109
DOI: 10.1055/s-0042-1759737
Original Article

Abnormalities of the Eyelashes in Turner's Syndrome

Layla Almarzooqi
1   Department of Pediatrics, Dr. von Hauner Children's Hospital, LMU Munich, Munich, Germany
,
Esther Schmidt
1   Department of Pediatrics, Dr. von Hauner Children's Hospital, LMU Munich, Munich, Germany
,
Heinrich Schmidt
1   Department of Pediatrics, Dr. von Hauner Children's Hospital, LMU Munich, Munich, Germany
,
Ilja Dubinski
1   Department of Pediatrics, Dr. von Hauner Children's Hospital, LMU Munich, Munich, Germany
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Abstract

Turner's syndrome (TS) is a sex chromosome disorder caused by a partial loss, complete absence or structural abnormality of one X chromosome in females. Special ocular features are often found. Some of the abnormalities are only cosmetic, such as the abnormalities of the eyelashes. The present prospective study with 12 TS and 12 control patients demonstrates the higher number of eyelashes as well as the greater vertical distance between the roots of the eyelashes in patients with TS compared with the control group. Increased awareness of this ophthalmological abnormality could be an additional diagnostic tool for early clinical suspicion of TS diagnosis.

Keywords

Turner's syndrome - ophthalmological - eyelashes - lymphedema

Ethical Standard

The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national guidelines on human experimentation and with the Declaration of Helsinki of 1975, as revised in 2008. All participating families gave their written consent for the photographs, the analysis, and the publication.




Publikationsverlauf

Eingereicht: 26. April 2022

Angenommen: 06. November 2022

Artikel online veröffentlicht:
22. Dezember 2022

© 2022. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 

  • References

  • 1 Denniston AK, Butler L. Ophthalmic features of Turner's syndrome. Eye (Lond) 2004; 18 (07) 680-684
    CrossrefPubMedSuche in Google Scholar
  • 2 Lessell S, Forbes AP. Eye signs in Turner's syndrome. Arch Ophthalmol 1966; 76 (02) 211-213
    CrossrefPubMedSuche in Google Scholar
  • 3 Thomas C, Cordier J, Reny A. Ophthalmic manifestations of Turner's syndrome [in French]. Arch Ophtalmol Rev Gen Ophtalmol 1969; 29 (06) 565-574
    PubMedSuche in Google Scholar
  • 4 Brunnerová R, Lebl J, Krásný J, Průhová S. Ocular manifestations in Turner's syndrome [in Czech]. Cesk Slov Oftalmol 2007; 63 (03) 176-184
    PubMedSuche in Google Scholar
  • 5 Huang J, Basith SST, Patel S. et al. Ocular findings in pediatric Turner syndrome. Ophthalmic Genet 2022; 43 (04) 450-453
    CrossrefPubMedSuche in Google Scholar
  • 6 Frangois J, Berger R, Saraux H. & Société Frangaise D'ophialmologie. (1972). Les Aberrations Chromosomiques en Ophtalmologie. In Rapport Présenté a la Société Frangaise D'Ophtalmologie le 9 Mai 1972 [in French]. Masson & Cie Editeurs, Paris, page 413
    PubMed
  • 7 Gellis SS, Feingold M, Southerland GR, Rogers JG. Picture of the month. Am J Dis Child 1978; 132 (04) 417-418
    PubMedSuche in Google Scholar
  • 8 Neel JV, Schull WJ. Human Heredity. Chicago: University of Chicago Press; 1954: 50-51
    Suche in Google Scholar