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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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Detalles Bibliográficos
Autores principales: Kenawy, Nihal, Pilz, Daniela T, Watts, Patrick
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2008
Materias:
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.
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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
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AT wattspatrick familialunilateralbrownsyndrome