rubinstein-taybi syndrome; a case report

نویسندگان

hadi sorkhi associate professor of nephrology, non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran

yasser asghari vostacolaee general physician, babol university of medical sciences, babol, iran

ali ghabeli juibari general physician, babol university of medical sciences, babol, iran

چکیده

objective rubinstein-taybi syndrome is a rare genetic disorder with characteristic featuresincluding downward slanting palpebral fissures, broad thumbs and halluces,and mental retardation. systemic features may involve cardiac, auditory,ophthalmic, endocrine, nervous, renal and respiratory systems. this syndromeis sporadic in nature and has been linked to microdeletion at 16p 13.3 encodingcreb-binding protein gene (crebbp). we report a 15-years-old girl, a knowncase of chronic renal failure, with downward slanting palpebral fissures towardthe ears, hypertelorism, short stature, beaked nose, micrognathia, strabismus,dental anomalies, large toes, broad thumbs, and mental retardation.

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Rubinstein-Taybi Syndrome: A Case Report

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عنوان ژورنال:
iranian journal of child neurology

جلد ۵، شماره ۲، صفحات ۳۹-۴۲

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