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Premature craniosynostosis in a rare genetic disease- A case report
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نویسنده
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dharamshi h.a. ,raza t. ,ali a.a.m. ,lilani z. ,ahsan s.z. ,faraz a. ,naqvi s.t.
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منبع
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iranian journal of public health - 2015 - دوره : 44 - شماره : 3 - صفحه:404 -406
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چکیده
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Background: crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete penetration and variable expressivity.its most notable characteristic feature is premature synostosis of cranial sutures the case presented is of a 4 yr old boy with box like head with microcephaly,protuberant eyes,hydrocephalus,low visual acquity diagnosed as a case of crouzon syndrome after clinical and radiological assessment. © 2015 iran j public health all right reserved.
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کلیدواژه
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Autosomal dominant; Crouzon syndrome; Premature craniosynostosis
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آدرس
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karachi medical and dental college, Pakistan, baqai medical college, Pakistan, sindh medical college/dow university of health sciences, Pakistan, karachi medical and dental college, Pakistan, sindh medical college/dow university of health sciences, Pakistan, karachi medical and dental college, Pakistan, karachi medical and dental college, Pakistan
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Authors
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