نتایج جستجو برای: cutaneous atrophy

تعداد نتایج: 90483  

Journal: :Parkinsonism & related disorders 2016
Wiebke Schrempf Istvan Katona Imis Dogan Verena V Felbert Miriam Wienecke Julia Heller Andrea Maier Andreas Hermann Katharina Linse Moritz D Brandt Heinz Reichmann Jörg B Schulz Johannes Schiefer Wolfgang H Oertel Alexander Storch Joachim Weis Kathrin Reetz

BACKGROUND Idiopathic rapid eye movement (REM) sleep behavior disorder (iRBD) has been increasingly acknowledged to be an initial specific manifestation of alpha-synucleinopathies such as Parkinson's disease (PD), multiple system atrophy (MSA) and dementia with Lewy bodies (DLB). Recent findings suggest that cutaneous abnormalities like small fiber neuropathy and alpha-synuclein deposition migh...

2004
R Morley

with small bowel sarcoidosis,3 the association between intestinal sarcoid and villous atrophy is unknown. Crohn's disease and sarcoidosis have common systemic manifestations, and the most frequently occurring cutaneous lesion to be associated with both conditions is erythema nodosum. However, cutaneous granulomas do occur in Crohn's disease, though rarely in areas which are not a direct extensi...

Journal: :Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie 2007
E F Georgescu Ligia Stănescu Daniela Dumitrescu Reanina Ionescu Iuliana Georgescu

UNLABELLED Sturge-Weber syndrome is a rare disorder consisting of a port-wine nevus in the distribution of the ophthalmic branch of the trigeminal nerve and central nervous system malformations. Facial cutaneous vascular malformation, seizures, and glaucoma are among the most common symptoms and signs. The syndrome results from malformation of the cerebral vasculature located within the pia mat...

Journal: :dental research journal 0
abhijeet sande mukund risbud avinash kshar arati oka paranjpe

progressive hemifacial atrophy, also known as parry-romberg syndrome, is an uncommon degenerative and poorly understood condition. it is characterized by a slow and progressive but self-limited atrophy affecting one side of the face. the incidence and the cause of this alteration are unknown. a cerebral disturbance of fat metabolism has been proposed as a primary cause. possible factors that ar...

Journal: :The Journal of biological chemistry 2000
H Yagyu T Kitamine J Osuga R Tozawa Z Chen Y Kaji T Oka S Perrey Y Tamura K Ohashi H Okazaki N Yahagi F Shionoiri Y Iizuka K Harada H Shimano H Yamashita T Gotoda N Yamada S Ishibashi

Acyl-CoA:cholesterol acyltransferase (ACAT) catalyzes esterification of cellular cholesterol. To investigate the role of ACAT-1 in atherosclerosis, we have generated ACAT-1 null (ACAT-1-/-) mice. ACAT activities were present in the liver and intestine but were completely absent in adrenal, testes, ovaries, and peritoneal macrophages in our ACAT-1-/- mice. The ACAT-1-/- mice had decreased openin...

2016
Waqas Ullah Hafez Mohammad A Abdullah Muhammad A Shahzad Muhammad Aslam Sadiq Ejaz Ahmad Sana Khan

Epidermal nevus syndrome (ENS) is a term used to describe the occurrence of an epidermal nevus in association with other extra-cutaneous developmental anomalies, most commonly involving the nervous and musculoskeletal systems. The nevus is classified on the basis of the main component which may be keratinocytic, sebaceous, follicular, apocrine, or eccrine. Most patients who present with ENS is ...

Journal: :AJNR. American journal of neuroradiology 2014
D D M Lin P B Barker H M Lederman T O Crawford

Ataxia-telangiectasia, an autosomal recessive disorder caused by defect of the ataxia-telangiectasia mutated gene, is characterized by progressive neurologic impairment with cerebellar atrophy, ocular and cutaneous telangiectasia, immunodeficiency, heightened sensitivity to ionizing radiation and susceptibility to developing lymphoreticular malignancy. Supratentorial brain abnormalities have be...

2014
Robert Fekete

INTRODUCTION Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder of DNA repair, with a prevalence of 1 in 1 million. It may also be a cause of neurological symptoms including sensorineural hearing loss, peripheral neuropathy, ataxia, and chorea. Severe neurological symptoms including mental retardation, short stature, and hypogonadism invoke De Sanctis-Cacchione syndrome (DCS). ...

Journal: :Actas dermo-sifiliograficas 2011
C Rodríguez-Caruncho I Bielsa

Lupus erythematosus tumidus (LET), a form of cutaneous lupus erythematosus that was described some years ago, has begun to receive more attention in the past decade as many published studies have helped to define the particularities of this subtype.The clinical features of LET include the absence of changes on the surface of the epidermis (such as erosion, atrophy, scaling, or follicular pluggi...

Journal: :iranian journal of parasitology 0
narges najafi eissa soleymani shahabeddin sarvi amirkeivan marofi anahita nosrati alireza davoodi

strongyloides stercoralis is a soil-transmitted helminth (sth) widespread in various part of the world. a 78-yr-old peasant diabetic female from mazandaran province northern iran, was admitted to infection department of the razi hospital in city of qaemshahr, north of iran complaining about abdominal skin rash, pruritus, itching, anorexia, nausea, vomiting, dysuria and cough. this patient had c...

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