سندرم شبه اسکلرودرمی معرفی یک بیمار نادر (سندرم ورنر)

Authors

محمدباقر اولیاء

m.b. owlia انوشه حقیقی

a. haghighi علی جوادزاده

a. javadzadeh

abstract

0

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

گزارش یک مورد سندرم POEMS با تظاهرات نادر بصورت هیپرتانسیون پولمونر و تظاهرات پوستی شبه اسکلرودرمی

          POEMS syndrome is a plasmocytic dyscrasia that consists a constellation    of polyneuropathy(p), organomegaly(o), endocrinopathy(e), monoclonal    gammapathy(m) and skin disorders(s).           Herein, we report a case of POEMS syndrome that was referred to  &nbsp...

full text

معرفی یک بیمار مبتلا به سندرم ایکتیوزلاملار

Introduction: Ichthyosis lamellar syndrome is a rare genodermatosis and in most families is inherited as an autosomal recessive trait because of transglutaminase-1 deficiency. Case Report: Our patient was a 6 year old girl and she was the result of consanguinity. She had large plate-like scales. The scales had mosaic-like pattern and erythroderma was absent. Tautness of her facial skin was as...

full text

معرفی یک بیمار مبتلا به سندرم مافوچی

Introduction: Maffucci syndrome is a rare clinical entity (approximately 200 cases have been reported in the medical literature) with a combination occurrence of multiple enchodroma and vascular tumors. Case Report: Our patient was an 18 year old girl born in a non-consanguineous marriage with finger and toe bones disorders (enchondroma) causing deformity of fingers and toes with multiple vas...

full text

My Resources

Save resource for easier access later


Journal title:
مجله علوم پزشکی رازی

جلد ۹، شماره ۳۲، صفحات ۶۳۷-۶۴۲

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023