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Familial unilateral Brown syndrome
We present a two-generation family with Brown syndrome. The proband was a six and a half-year-old female who presented with a history of failure of dextro-elevation of her left eye. A full ophthalmic evaluation was consistent with a left Brown syndrome. Family history revealed that her mother was op...
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2636128/ https://www.ncbi.nlm.nih.gov/pubmed/18711279 |
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author | Kenawy, Nihal Pilz, Daniela T Watts, Patrick |
author_facet | Kenawy, Nihal Pilz, Daniela T Watts, Patrick |
author_sort | Kenawy, Nihal |
collection | PubMed |
description | We present a two-generation family with Brown syndrome. The proband was a six and a half-year-old female who presented with a history of failure of dextro-elevation of her left eye. A full ophthalmic evaluation was consistent with a left Brown syndrome. Family history revealed that her mother was operated on as a child for left Brown syndrome and examination of her four and a half-year-old sibling showed similar affection in the left eye. Autosomal dominant inheritance has been postulated in this condition. To our knowledge this is the first report of three members of a two-generation family with left-sided Brown syndrome. Genetic counseling of Brown syndrome cases is advised; nevertheless, identification of the responsible gene should shed more light on its genetics. |
format | Text |
id | pubmed-2636128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-26361282009-02-10 Familial unilateral Brown syndrome Kenawy, Nihal Pilz, Daniela T Watts, Patrick Indian J Ophthalmol Brief Communication We present a two-generation family with Brown syndrome. The proband was a six and a half-year-old female who presented with a history of failure of dextro-elevation of her left eye. A full ophthalmic evaluation was consistent with a left Brown syndrome. Family history revealed that her mother was operated on as a child for left Brown syndrome and examination of her four and a half-year-old sibling showed similar affection in the left eye. Autosomal dominant inheritance has been postulated in this condition. To our knowledge this is the first report of three members of a two-generation family with left-sided Brown syndrome. Genetic counseling of Brown syndrome cases is advised; nevertheless, identification of the responsible gene should shed more light on its genetics. Medknow Publications 2008 /pmc/articles/PMC2636128/ /pubmed/18711279 Text en |
spellingShingle | Brief Communication Kenawy, Nihal Pilz, Daniela T Watts, Patrick Familial unilateral Brown syndrome |
title | Familial unilateral Brown syndrome |
title_full | Familial unilateral Brown syndrome |
title_fullStr | Familial unilateral Brown syndrome |
title_full_unstemmed | Familial unilateral Brown syndrome |
title_short | Familial unilateral Brown syndrome |
title_sort | familial unilateral brown syndrome |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2636128/ https://www.ncbi.nlm.nih.gov/pubmed/18711279 |
work_keys_str_mv | AT kenawynihal familialunilateralbrownsyndrome AT pilzdanielat familialunilateralbrownsyndrome AT wattspatrick familialunilateralbrownsyndrome |