نتایج جستجو برای: macrodactyly

تعداد نتایج: 104  

Journal: :Acta medica 2010
Shalimar Abdullah Nor Hazla Mohd Haflah Jamari Sapuan Srijit Das

We present a 20-year-old Malay male whom we believe has Proteus syndrome, a rare congenital disorder of asymmetrical overgrowth of body tissues. There are fewer than 100 confirmed cases reported worldwide thus the clinical presentation and histopathological findings are of significance. Our patient presented with an overgrown right small finger and subcutaneous purplish pigmentation over his le...

Journal: :بینا 0
احمد میرشاهی a mirshahi تهران- میدان قزوین- بیمارستان فارابی- مرکز تحقیقات چشم دانشگاه علوم پزشکی تهران آرش میرمحمدصادقی a mir mohammad sadeghi شهرستان خوانسار تاریخ لادن اسپندار l espandar

purpose: to report a case of proteus syndrome with new ophthalmic findings not reported elsewhere. patient and findings: the patient is an 18-year-old girl with red lesions on hand and foot from birth and disproportionate growth of right upper and lower limbs from the first year of life. on examination, the patient has enlargement of the right upper and lower limb, macrodactyly, vascular malfor...

Journal: :Anais brasileiros de dermatologia 2011
Hiram Larangeira de Almeida Roberto Coswig Fiss Rudolf Happle

The Proteus syndrome was described 1983 . It has asymmetric gigantism of the limbs, verrucous epidermal naevi, cerebriform enlargement of the plantar region, vascular malformations and neoplasms, as lipomas. It received this denomination after Proteus from the Greek mythology, who had the ability to change his form . A 15 year-old boy, reported a congenital hypertrophy with syndactily of the se...

2011
Elpis Mantadakis Savvas Deftereos Efthimios Sivridis Lambros Michailidis Athanassios Chatzimichael Panos Prassopoulos

Introduction: Macrodystrophia lipomatosa (MDL) is a non-hereditary congenital developmental anomaly characterized by localized gigantism due to overgrowth of all mesenchymal elements. Case Report: The authors describe a case of macrodystrophia lipomatosa (MDL) with involvement of the median nerve in a 10-year-old girl and review the pathologic, radiographic, ultrasonographic and MR imaging char...

Journal: :iranian journal of child neurology 0
farhad heydarian md, associate professor of pediatrics, mashhad university of medical sciences, mashhad, iran farah ashrafzadeh md, pediatric neurologist,professor of pediatrics, mashhad university of medical sciences,mashhad, iran mahmoud taheri heravi associate professor of radiology, mashhad university of medical sciences,mashhad, iran

objective proteus syndrome is an extremely rare, sporadic and progressive disorder. we describe a four-month-old male baby with central nervous system manifestations in this article. clinical presentation a four-month-old boy was admitted into our hospital with three tonic - clonic generalized seizure attacks which started from the day before admission. each seizure attack lasted less than 10 m...

2012
Mozhgan Hashemieh Bahar Mansoori Reza Tavakoli Koroush Sheibani

BACKGROUND Proteus syndrome is a very rare condition with less than 100 confirmed cases reported worldwide. We report a case of Proteus syndrome in a two-year-old male who has hemophilia A comorbidity. CASE PRESENTATION A two-year-old male patient was admitted with the chief complaint of severe bleeding in mouth cavity after trauma for two weeks. At admission he was found to have petechiae on...

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